-
2
-
-
0031262268
-
Endocrine and nutritional regulation of prenatal growth
-
Gluckman PD. Endocrine and nutritional regulation of prenatal growth. Acta Paediatrica 1997; 423 (supplement): 153-157.
-
(1997)
Acta Paediatrica
, vol.423
, Issue.SUPPL.
, pp. 153-157
-
-
Gluckman, P.D.1
-
4
-
-
0031849328
-
Growth factors and the regulation of fetal growth
-
Hill DJ, Petrik J & Arany E. Growth factors and the regulation of fetal growth. Diabetes Care 1998; 21 (supplment 2): B60-B69.
-
(1998)
Diabetes Care
, vol.21
, Issue.SUPPL. 2
-
-
Hill, D.J.1
Petrik, J.2
Arany, E.3
-
5
-
-
0032976345
-
Mechanisms of in utero overgrowth
-
D'Ercole AJ. Mechanisms of in utero overgrowth. Acta Paediatrica 1999; 88 (supplment): 31-36.
-
(1999)
Acta Paediatrica
, vol.88
, Issue.SUPPL.
, pp. 31-36
-
-
D'Ercole, A.J.1
-
6
-
-
85047682715
-
Minireview: Tissue-specific versus generalized gene targeting of the igfl and igflr genes and their roles in insulin-like growth factor physiology
-
Butler AA & LeRoith D. Minireview: tissue-specific versus generalized gene targeting of the igfl and igflr genes and their roles in insulin-like growth factor physiology. Endocrinology 2001; 142: 1685-1688.
-
(2001)
Endocrinology
, vol.142
, pp. 1685-1688
-
-
Butler, A.A.1
LeRoith, D.2
-
7
-
-
0011327707
-
Insulin-like growth factor control of growth: Insights from targeted disruption of murine genes and from human disease
-
In Handwerger S (ed.); Totowa, New Jersey: Humana Press
-
Chernausek S. Insulin-like growth factor control of growth: insights from targeted disruption of murine genes and from human disease. In Handwerger S (ed.) Molecular and Cellular Pediatric Endocrinology pp 11-22. Totowa, New Jersey: Humana Press, 1999.
-
(1999)
Molecular and Cellular Pediatric Endocrinology
, pp. 11-22
-
-
Chernausek, S.1
-
8
-
-
0030735169
-
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
-
Sun FL, Dean WL, Kelsey G et al. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. Nature 1997; 389: 809-815.
-
(1997)
Nature
, vol.389
, pp. 809-815
-
-
Sun, F.L.1
Dean, W.L.2
Kelsey, G.3
-
9
-
-
0030221121
-
Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igflr null backgrounds
-
Ludwig T, Eggenschwiler J, Fisher P et al. Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igflr null backgrounds. Developmental Biology 1996; 177: 517-535.
-
(1996)
Developmental Biology
, vol.177
, pp. 517-535
-
-
Ludwig, T.1
Eggenschwiler, J.2
Fisher, P.3
-
10
-
-
0028575985
-
Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
-
Lau MM, Stewart CE, Liu Z et al. Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes & Development 1994; 8: 2953-2963.
-
(1994)
Genes & Development
, vol.8
, pp. 2953-2963
-
-
Lau, M.M.1
Stewart, C.E.2
Liu, Z.3
-
11
-
-
0029917507
-
Fibroblast growth factor receptor 3 is a negative regulator of bone growth
-
Deng C, Wynshaw-Boris A, Zhou F et al. Fibroblast growth factor receptor 3 is a negative regulator of bone growth. Cell 1996; 84: 911-921.
-
(1996)
Cell
, vol.84
, pp. 911-921
-
-
Deng, C.1
Wynshaw-Boris, A.2
Zhou, F.3
-
12
-
-
0030883748
-
Translocations involving 4p16.3 in three families: Deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome
-
Partington MW, Fagan K, Soubjaki V & Turner G. Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome. Journal of Medical Genetics 1997; 34: 719-728.
-
(1997)
Journal of Medical Genetics
, vol.34
, pp. 719-728
-
-
Partington, M.W.1
Fagan, K.2
Soubjaki, V.3
Turner, G.4
-
13
-
-
0032509990
-
Location of enhancers is essential for the imprinting of H19 and Igf2 genes
-
Webber AL, Ingram RS, Levorse JM & Tilghman SM. Location of enhancers is essential for the imprinting of H19 and Igf2 genes. Nature 1998; 391: 711-715.
-
(1998)
Nature
, vol.391
, pp. 711-715
-
-
Webber, A.L.1
Ingram, R.S.2
Levorse, J.M.3
Tilghman, S.M.4
-
14
-
-
0021679240
-
Serum levels of insulin-like growth factor (IGF) and IGF binding protein in constitutionally tall children and adolescents
-
Gourmelen M, Le Bouc Y, Girard F & Binoux M. Serum levels of insulin-like growth factor (IGF) and IGF binding protein in constitutionally tall children and adolescents. Journal of Clinical Endocrinology and Metabolism 1984; 59: 1197-1203.
-
(1984)
Journal of Clinical Endocrinology and Metabolism
, vol.59
, pp. 1197-1203
-
-
Gourmelen, M.1
Le Bouc, Y.2
Girard, F.3
Binoux, M.4
-
15
-
-
0028143234
-
Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man
-
Smith EP, Boyd J, Frank GR et al. Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man. New England Journal of Medicine 1994; 331: 1056-1061.
-
(1994)
New England Journal of Medicine
, vol.331
, pp. 1056-1061
-
-
Smith, E.P.1
Boyd, J.2
Frank, G.R.3
-
16
-
-
0028792229
-
Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens
-
Morishima A, Grumbach MM, Simpson ER et al. Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens. Journal of Clinical Endocrinology and Metabolism 1995; 80: 3689-3698.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 3689-3698
-
-
Morishima, A.1
Grumbach, M.M.2
Simpson, E.R.3
-
17
-
-
0030940217
-
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
-
Rao E, Weiss B, Fukami M et al. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nature Genetics 1997; 16: 54-63.
-
(1997)
Nature Genetics
, vol.16
, pp. 54-63
-
-
Rao, E.1
Weiss, B.2
Fukami, M.3
-
18
-
-
0030877094
-
PHOG, a candidate gene for involvement in the short stature of Turner syndrome
-
Ellison JW, Wardak Z, Young MF et al. PHOG, a candidate gene for involvement in the short stature of Turner syndrome. Human Molecular Genetics 1997; 6: 1341-1347.
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 1341-1347
-
-
Ellison, J.W.1
Wardak, Z.2
Young, M.F.3
-
19
-
-
0035133355
-
SHOX haploinsufficiency and overdosage: Impact of gonadal function status
-
Ogata T, Matsuo N & Nishimura G. SHOX haploinsufficiency and overdosage: impact of gonadal function status. Journal of Medical Genetics 2001; 38: 1-6.
-
(2001)
Journal of Medical Genetics
, vol.38
, pp. 1-6
-
-
Ogata, T.1
Matsuo, N.2
Nishimura, G.3
-
20
-
-
0035131335
-
Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome
-
Binder G, Eggermann T, Enders H et al. Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome. Journal of Pediatrics 2001; 138: 285-287.
-
(2001)
Journal of Pediatrics
, vol.138
, pp. 285-287
-
-
Binder, G.1
Eggermann, T.2
Enders, H.3
-
21
-
-
0034841584
-
Significant population variation in adult male height associated with the Y chromosome and the aromatase gene
-
Ellis JA, Stebbing M & Harrap SB. Significant population variation in adult male height associated with the Y chromosome and the aromatase gene. Journal of Clinical Endocrinology and Metabolism 2001; 86: 4147-4150.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 4147-4150
-
-
Ellis, J.A.1
Stebbing, M.2
Harrap, S.B.3
-
24
-
-
0016769824
-
Measurement of thoracic spine length on chest radiographs of newborn infants
-
Kuhns LR & Holt JF. Measurement of thoracic spine length on chest radiographs of newborn infants. Radiology 1975; 116: 395-197.
-
(1975)
Radiology
, vol.116
, pp. 395-397
-
-
Kuhns, L.R.1
Holt, J.F.2
-
27
-
-
0028233104
-
Epidemiological analysis of outcomes of pregnancy in diabetic mothers: Identification of the most characteristic and most frequent congenital anomalies
-
Martinez-Frias ML. Epidemiological analysis of outcomes of pregnancy in diabetic mothers: identification of the most characteristic and most frequent congenital anomalies. American Journal of Medical Genetics 1994; 51: 108-113.
-
(1994)
American Journal of Medical Genetics
, vol.51
, pp. 108-113
-
-
Martinez-Frias, M.L.1
-
28
-
-
0021484936
-
Congenital malformation in offspring of diabetics
-
Neave C. Congenital malformation in offspring of diabetics. Perspectives in Pediatric Pathology 1984; 8: 213-222.
-
(1984)
Perspectives in Pediatric Pathology
, vol.8
, pp. 213-222
-
-
Neave, C.1
-
31
-
-
0015989659
-
A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly
-
Weaver DD, Graham CB, Thomas IT & Smith DW. A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly. Journal of Pediatrics 1974; 84: 547-552.
-
(1974)
Journal of Pediatrics
, vol.84
, pp. 547-552
-
-
Weaver, D.D.1
Graham, C.B.2
Thomas, I.T.3
Smith, D.W.4
-
32
-
-
0031041271
-
Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor
-
Dunne MJ, Kane C, Shepherd RM et al. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor. New England Journal of Medicine 1997; 336: 703-706.
-
(1997)
New England Journal of Medicine
, vol.336
, pp. 703-706
-
-
Dunne, M.J.1
Kane, C.2
Shepherd, R.M.3
-
33
-
-
0029756638
-
Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas PM, Wohllk N, Huang E et al. Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy. American Journal of Human Genetics 1996; 59: 510-518.
-
(1996)
American Journal of Human Genetics
, vol.59
, pp. 510-518
-
-
Thomas, P.M.1
Wohllk, N.2
Huang, E.3
-
34
-
-
0023635185
-
Edema associated with improved glycemic control in an adolescent with type 1 diabetes
-
Sharon M, Cassoria FG, Rose SR & Loriaux DL. Edema associated with improved glycemic control in an adolescent with type 1 diabetes. Journal of Pediatrics 1987; 111: 403-404.
-
(1987)
Journal of Pediatrics
, vol.111
, pp. 403-404
-
-
Sharon, M.1
Cassoria, F.G.2
Rose, S.R.3
Loriaux, D.L.4
-
35
-
-
0031041271
-
Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor
-
Dunne MJ, Kane C, Shepherd RM et al. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor. New England Journal of Medicine 1997; 336: 703-706.
-
(1997)
New England Journal of Medicine
, vol.336
, pp. 703-706
-
-
Dunne, M.J.1
Kane, C.2
Shepherd, R.M.3
-
36
-
-
0028972501
-
Reconstitution of IKATP: An inward rectifier subunit plus the sulfonylurea receptor
-
(see comments)
-
Inagaki N, Gonoi T, Clement JP et al. Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor (see comments). Science 1995; 270: 1166-1170.
-
(1995)
Science
, vol.270
, pp. 1166-1170
-
-
Inagaki, N.1
Gonoi, T.2
Clement, J.P.3
-
37
-
-
0032190017
-
Paternal mutation of the sulfonylurea receptor (SURI) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
-
Verkarre V, Fournet JC, De Lonlay P et al. Paternal mutation of the sulfonylurea receptor (SURI) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. Journal of Clinical Investigation 1998; 102: 1286-1291.
-
(1998)
Journal of Clinical Investigation
, vol.102
, pp. 1286-1291
-
-
Verkarre, V.1
Fournet, J.C.2
De Lonlay, P.3
-
38
-
-
0031942583
-
Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant
-
(see comments)
-
Thornton PS, Satin-Smith MS, Herold K et al. Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant (see comments). Journal of Pediatrics 1998; 132: 9-14.
-
(1998)
Journal of Pediatrics
, vol.132
, pp. 9-14
-
-
Thornton, P.S.1
Satin-Smith, M.S.2
Herold, K.3
-
39
-
-
0032556969
-
Familial hyperinsulinism caused by an activating glucokinase mutation
-
Glaser B, Kesavan P, Heyman M et al. Familial hyperinsulinism caused by an activating glucokinase mutation. New England Journal of Medicine 1998; 338 226-230.
-
(1998)
New England Journal of Medicine
, vol.338
, pp. 226-230
-
-
Glaser, B.1
Kesavan, P.2
Heyman, M.3
-
40
-
-
0032493123
-
Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
-
Stanley CA, Lieu YK, Hsu BY et al. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. New England Journal of Medicine 1998; 338: 1352-1357.
-
(1998)
New England Journal of Medicine
, vol.338
, pp. 1352-1357
-
-
Stanley, C.A.1
Lieu, Y.K.2
Hsu, B.Y.3
-
41
-
-
0031942583
-
Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant
-
Thornton PS, Satin-Smith MS, Herold K et al. Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant. Journal of Pediatrics 1998; 132: 9-14.
-
(1998)
Journal of Pediatrics
, vol.132
, pp. 9-14
-
-
Thornton, P.S.1
Satin-Smith, M.S.2
Herold, K.3
-
42
-
-
0031093810
-
Overgrowth. Section VI. Genetic syndromes and other disorders associated with overgrowth
-
Sotos JF. Overgrowth. Section VI. Genetic syndromes and other disorders associated with overgrowth. Clinical Pediatrics (Philadelphia) 1997; 36: 157-170.
-
(1997)
Clinical Pediatrics (Philadelphia)
, vol.36
, pp. 157-170
-
-
Sotos, J.F.1
-
44
-
-
0022910322
-
Wiedemann-Beckwith syndrome: Presentation of clinical and cytogenetic data on 22 new cases and review of the literature
-
Pettenati MJ, Haines JL, Higgins RR et al. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Human Genetics 1986; 74: 143-154.
-
(1986)
Human Genetics
, vol.74
, pp. 143-154
-
-
Pettenati, M.J.1
Haines, J.L.2
Higgins, R.R.3
-
45
-
-
0033975096
-
Beckwith-Wiedemann syndrome: Imprinting inclusters revisited
-
Maher ER & Reik W. et al. Beckwith-Wiedemann syndrome: imprinting inclusters revisited. Journal of Clinical Investigation 2000; 105(3): 247-252.
-
(2000)
Journal of Clinical Investigation
, vol.105
, Issue.3
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
47
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
-
Weksberg R, Shen DR, Fei YL et al. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nature Genetics 1993; 5: 143-150.
-
(1993)
Nature Genetics
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, L.3
-
49
-
-
0028124711
-
Clinical features and natural history of Beckwith-Wiedemann syndrome: Presentation of 74 new cases
-
Elliott M, Bayly R, Cole T et al. Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases. Clinical Genetics 1994; 46: 168-174.
-
(1994)
Clinical Genetics
, vol.46
, pp. 168-174
-
-
Elliott, M.1
Bayly, R.2
Cole, T.3
-
51
-
-
0031031959
-
Frequency of Wiedemann-Beckwith syndrome in Germany; Rate of hemihyperplasia and of tumours in affected children
-
Wiedemann HR. Frequency of Wiedemann-Beckwith syndrome in Germany; rate of hemihyperplasia and of tumours in affected children. European Journal of Pediatrics 1997; 156: 251.
-
(1997)
European Journal of Pediatrics
, vol.156
, pp. 251
-
-
Wiedemann, H.R.1
-
52
-
-
0023682883
-
Simpson-Golabi-Behmel syndrome: An X-linked encephalo-trophoschisis syndrome
-
Neri G, Marini R, Cappa M et al. Simpson-Golabi-Behmel syndrome: an X-linked encephalo-trophoschisis syndrome. American Journal of Medical Genetics 1988; 30; 287-299.
-
(1988)
American Journal of Medical Genetics
, vol.30
, pp. 287-299
-
-
Neri, G.1
Marini, R.2
Cappa, M.3
-
54
-
-
13344261391
-
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
-
Pilia G, Hughes-Benzie RM, MacKenzie A et al. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nature Genetics 1996; 12: 241-247.
-
(1996)
Nature Genetics
, vol.12
, pp. 241-247
-
-
Pilia, G.1
Hughes-Benzie, R.M.2
MacKenzie, A.3
-
56
-
-
0023017259
-
Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies
-
Perlman M. Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism, and multiple congenital anomalies. American Journal of Medical Genetics 1986; 25: 793-795.
-
(1986)
American Journal of Medical Genetics
, vol.25
, pp. 793-795
-
-
Perlman, M.1
-
58
-
-
0014973195
-
Syndrome of accelerated skeletal maturation and relative failure to thrive: A newly recognized clinical growth disorder
-
Marshall RE, Graham CB, Scott CR & Smith DW. Syndrome of accelerated skeletal maturation and relative failure to thrive: a newly recognized clinical growth disorder. Journal of Pediatrics 1971; 78: 95-101.
-
(1971)
Journal of Pediatrics
, vol.78
, pp. 95-101
-
-
Marshall, R.E.1
Graham, C.B.2
Scott, C.R.3
Smith, D.W.4
-
62
-
-
0016923905
-
Diagnostic problems in cerebral gigantism
-
(letter)
-
Cohen MM. Diagnostic problems in cerebral gigantism (letter) Journal of Medical Genetics 1976; 13: 80.
-
(1976)
Journal of Medical Genetics
, vol.13
, pp. 80
-
-
Cohen, M.M.1
-
66
-
-
0034667671
-
Familial patterns of covariation for cardiovascular risk factors in adults: The Victorian Family Heart Study
-
Harrap SB, Stebbing M, Hopper JL et al. Familial patterns of covariation for cardiovascular risk factors in adults: The Victorian Family Heart Study. American Journal of Epidemiology 2000; 152: 704-715.
-
(2000)
American Journal of Epidemiology
, vol.152
, pp. 704-715
-
-
Harrap, S.B.1
Stebbing, M.2
Hopper, J.L.3
-
68
-
-
0024356245
-
Correlation of the parameters of 24-hour growth hormone secretion with growth velocity in 93 children of varying height
-
Rochiccioli P, Messina A, Tauber MT & Enjaume C. Correlation of the parameters of 24-hour growth hormone secretion with growth velocity in 93 children of varying height. Hormone Research 1989; 31: 115-118.
-
(1989)
Hormone Research
, vol.31
, pp. 115-118
-
-
Rochiccioli, P.1
Messina, A.2
Tauber, M.T.3
Enjaume, C.4
-
70
-
-
0028182879
-
Growth hormone secretion in children and adolescents with familial tall stature
-
Tauber M, Pienkowski C & Rochiccioli P. Growth hormone secretion in children and adolescents with familial tall stature. European Journal of Pediatrics 1994; 153: 311-316.
-
(1994)
European Journal of Pediatrics
, vol.153
, pp. 311-316
-
-
Tauber, M.1
Pienkowski, C.2
Rochiccioli, P.3
-
71
-
-
0021234745
-
The pattern of growth in children with constitutional tall stature from birth to age 9 years. A longitudinal study
-
Dickerman Z, Loewinger J & Laron Z. The pattern of growth in children with constitutional tall stature from birth to age 9 years. A longitudinal study. Acta Paediatrica Scandinavica 1984; 73: 530-536.
-
(1984)
Acta Paediatrica Scandinavica
, vol.73
, pp. 530-536
-
-
Dickerman, Z.1
Loewinger, J.2
Laron, Z.3
-
73
-
-
0023350956
-
Height and occupational success: A review and critique
-
Hensley WE & Cooper R. Height and occupational success: a review and critique. Psychology Reports 1987; 60: 843-849.
-
(1987)
Psychology Reports
, vol.60
, pp. 843-849
-
-
Hensley, W.E.1
Cooper, R.2
-
74
-
-
0026023362
-
Intelligence and educational level in adult males at the extremes of stature
-
Teasdale TW, Owen DR & Sorensen TI. Intelligence and educational level in adult males at the extremes of stature. Human Biology 1991; 63: 19-30.
-
(1991)
Human Biology
, vol.63
, pp. 19-30
-
-
Teasdale, T.W.1
Owen, D.R.2
Sorensen, T.I.3
-
75
-
-
0031453005
-
Outcome in tall stature. Final height and psychological aspects in 220 patients with and without treatment
-
Binder G, Grauer ML, Wehner AV et al. Outcome in tall stature. Final height and psychological aspects in 220 patients with and without treatment. European Journal of Pediatrics 1997; 156: 905-910.
-
(1997)
European Journal of Pediatrics
, vol.156
, pp. 905-910
-
-
Binder, G.1
Grauer, M.L.2
Wehner, A.V.3
-
76
-
-
0016666157
-
Tall girls: A survey of 15 years of management and treatment
-
Wettenhall HN, Cahill C & Roche AF. Tall girls: a survey of 15 years of management and treatment. Journal of Pediatrics 1975; 86: 602-610.
-
(1975)
Journal of Pediatrics
, vol.86
, pp. 602-610
-
-
Wettenhall, H.N.1
Cahill, C.2
Roche, A.F.3
-
77
-
-
0018218685
-
Treatment of excessively tall girls and boys with sex hormones
-
Prader A & Zachmann M. Treatment of excessively tall girls and boys with sex hormones. Pediatrics 1978; 62: 1202-1210.
-
(1978)
Pediatrics
, vol.62
, pp. 1202-1210
-
-
Prader, A.1
Zachmann, M.2
-
79
-
-
29444450289
-
Tables for predicting adult height from skeletal age: Revised for use with the Greulich-Pyle hand standards
-
Bayley N. Tables for predicting adult height from skeletal age: revised for use with the Greulich-Pyle hand standards. Journal of Pediatrics 1952; 40: 432-441.
-
(1952)
Journal of Pediatrics
, vol.40
, pp. 432-441
-
-
Bayley, N.1
-
81
-
-
0029927849
-
Accuracy of final height prediction and effect of growth-reductive therapy in 362 constitutionally tall children
-
de Waal WJ, Greyn-Fokker MH, Stijnen T et al. Accuracy of final height prediction and effect of growth-reductive therapy in 362 constitutionally tall children. Journal of Clinical Endocrinology and Metabolism 1996; 81: 1206-1216.
-
(1996)
Journal of Clinical Endocrinology and Metabolism
, vol.81
, pp. 1206-1216
-
-
De Waal, W.J.1
Greyn-Fokker, M.H.2
Stijnen, T.3
-
82
-
-
0030404316
-
A new model to predict final height in constitutionally tall children
-
de Waal WJ, Stijnen T, Lucas IS et al. A new model to predict final height in constitutionally tall children. Acta Paediatrica 1996; 85: 889-893.
-
(1996)
Acta Paediatrica
, vol.85
, pp. 889-893
-
-
De Waal, W.J.1
Stijnen, T.2
Lucas, I.S.3
-
83
-
-
0029060778
-
The role of estrogen in pubertal skeletal physiology: Epiphyseal maturation and mineralization of the skeleton
-
Frank GR. The role of estrogen in pubertal skeletal physiology: epiphyseal maturation and mineralization of the skeleton. Acta Paediatrica 1995; 84: 627-630.
-
(1995)
Acta Paediatrica
, vol.84
, pp. 627-630
-
-
Frank, G.R.1
-
86
-
-
0023771481
-
The results of short-term (6 months) high-dose testosterone treatment on bone age and adult height in boys of excessively tall stature
-
Bramswig JH, von Lengerke HJ, Schmidt H & Schellong G. The results of short-term (6 months) high-dose testosterone treatment on bone age and adult height in boys of excessively tall stature. European Journal of Pediatrics 1988; 148: 104-106.
-
(1988)
European Journal of Pediatrics
, vol.148
, pp. 104-106
-
-
Bramswig, J.H.1
Von Lengerke, H.J.2
Schmidt, H.3
Schellong, G.4
-
87
-
-
0022459512
-
Testosterone treatment of constitutional delay in growth and development: Effect of dose on predicted versus definitive height
-
Martin MM, Martin AL & Mossman KL. Testosterone treatment of constitutional delay in growth and development: effect of dose on predicted versus definitive height. Acta Endocrinologica (Copenhagen) 1986; 279(supplement): 147-152.
-
(1986)
Acta Endocrinologica (Copenhagen)
, vol.279
, Issue.SUPPL.
, pp. 147-152
-
-
Martin, M.M.1
Martin, A.L.2
Mossman, K.L.3
-
88
-
-
0029021102
-
High dose testosterone therapy for reduction of final height in constitutionally tall boys: Does it influence testicular function in adulthood?
-
de Waal WJ, Vreeburg JT, Bekkering F et al. High dose testosterone therapy for reduction of final height in constitutionally tall boys: does it influence testicular function in adulthood? Clinical Endocrinology (Oxford) 1995; 43: 87-95.
-
(1995)
Clinical Endocrinology (Oxford)
, vol.43
, pp. 87-95
-
-
De Waal, W.J.1
Vreeburg, J.T.2
Bekkering, F.3
-
89
-
-
0018745903
-
The functional state of the hypothalamo-pituitary axis after high-dose oestrogen therapy in excessively tall girls
-
Hanker JP, Schellong G & Schneider HP. The functional state of the hypothalamo-pituitary axis after high-dose oestrogen therapy in excessively tall girls. Acta Endocrinologica (Copenhagen) 1979; 91: 19-29.
-
(1979)
Acta Endocrinologica (Copenhagen)
, vol.91
, pp. 19-29
-
-
Hanker, J.P.1
Schellong, G.2
Schneider, H.P.3
-
90
-
-
0028784090
-
Long term sequelae of sex steroid treatment in the management of constitutionally tall stature
-
de Waal WJ, Torn M, de Muinck Keizer-Schrama et al. Long term sequelae of sex steroid treatment in the management of constitutionally tall stature. Archives of Disease in Childhood 1995; 73: 311-315.
-
(1995)
Archives of Disease in Childhood
, vol.73
, pp. 311-315
-
-
De Waal, W.J.1
Torn, M.2
De Muinck Keizer-Schrama3
-
91
-
-
85031366765
-
Tall girls
-
February 5, 2002.
-
France D. Tall girls. Newsweek. MSNB.com, February 5, 2002.
-
Newsweek
-
-
France, D.1
-
92
-
-
0026099536
-
Estrogen treatment of tall girls: Dose dependency of effects on subsequent growth and IGF-I levels in blood
-
Svan H, Ritzen EM, Hall K & Johansson L. Estrogen treatment of tall girls: dose dependency of effects on subsequent growth and IGF-I levels in blood. Acta Paediatrica Scandinavica 1991; 80: 328-332.
-
(1991)
Acta Paediatrica Scandinavica
, vol.80
, pp. 328-332
-
-
Svan, H.1
Ritzen, E.M.2
Hall, K.3
Johansson, L.4
-
99
-
-
0023250788
-
Reduced growth hormone response to growth hormone-releasing hormone in children with simple obesity: Evidence for somatomedin-C mediated inhibition
-
Loche S, Cappa M, Borrelli P et al. Reduced growth hormone response to growth hormone-releasing hormone in children with simple obesity: evidence for somatomedin-C mediated inhibition. Clinical Endocrinology (Oxford) 1987; 27: 145-153.
-
(1987)
Clinical Endocrinology (Oxford)
, vol.27
, pp. 145-153
-
-
Loche, S.1
Cappa, M.2
Borrelli, P.3
-
100
-
-
0032829033
-
Monogenic disorders of obesity and body fat distribution
-
Chen D & Garg A. Monogenic disorders of obesity and body fat distribution. Journal of Lipid Research 1999; 40: 1735-1746.
-
(1999)
Journal of Lipid Research
, vol.40
, pp. 1735-1746
-
-
Chen, D.1
Garg, A.2
-
101
-
-
0030878110
-
Congenital leptin deficiency is associated with severe early-onset obesity in humans
-
Montague CT, Farooqi IS, Whitehead JP et al. Congenital leptin deficiency is associated with severe early-onset obesity in humans. Nature 1997; 387: 903-908.
-
(1997)
Nature
, vol.387
, pp. 903-908
-
-
Montague, C.T.1
Farooqi, I.S.2
Whitehead, J.P.3
-
102
-
-
0032014836
-
A leptin missense mutation associated with hypogonadism and morbid obesity
-
Strobel S, Issad T, Camoin L et al. A leptin missense mutation associated with hypogonadism and morbid obesity. Nature Genetics 1998; 18: 213-215.
-
(1998)
Nature Genetics
, vol.18
, pp. 213-215
-
-
Strobel, S.1
Issad, T.2
Camoin, L.3
-
103
-
-
0344450708
-
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
-
Clement K, Vaisse C, Lahlou N, et al. A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction. Nature 1998; 392: 398-401.
-
(1998)
Nature
, vol.392
, pp. 398-401
-
-
Clement, K.1
Vaisse, C.2
Lahlou, N.3
-
104
-
-
0030949271
-
Obesity and impaired prohormone processing associated with mutations in the human prohormone covertase I gene
-
Jackson RS, Creemers JW, Ohagi S et al. Obesity and impaired prohormone processing associated with mutations in the human prohormone covertase I gene. Nature Genetics 1997; 16: 303-306.
-
(1997)
Nature Genetics
, vol.16
, pp. 303-306
-
-
Jackson, R.S.1
Creemers, J.W.2
Ohagi, S.3
-
105
-
-
0031838353
-
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
-
Krude H, Biebermann H, Luck W et al. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nature Genetics 1998; 19: 155-157.
-
(1998)
Nature Genetics
, vol.19
, pp. 155-157
-
-
Krude, H.1
Biebermann, H.2
Luck, W.3
-
106
-
-
0033927916
-
Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity
-
Vaisse C, Clement K, Durand E et al. Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity. Journal of Clinical Investigation 2000; 106: 253-262.
-
(2000)
Journal of Clinical Investigation
, vol.106
, pp. 253-262
-
-
Vaisse, C.1
Clement, K.2
Durand, E.3
-
107
-
-
0343953074
-
Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency
-
Farooqi IS, Yeo GS, Keogh JM et al. Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency. Journal of Clinical Investigation 2000; 106: 271-279.
-
(2000)
Journal of Clinical Investigation
, vol.106
, pp. 271-279
-
-
Farooqi, I.S.1
Yeo, G.S.2
Keogh, J.M.3
-
108
-
-
0011371668
-
Somatotroph adenomas: Acromegaly and gigantism
-
In Thapar K, Kovacs K, Scheithauer BW & Lloyd RV (eds); Totowa, New Jersey: Humana Press
-
Quabbe H-J & Plockinger U. Somatotroph adenomas: acromegaly and gigantism. In Thapar K, Kovacs K, Scheithauer BW & Lloyd RV (eds) Diagnosis and Management of Pituitary Tumours pp 295-316. Totowa, New Jersey: Humana Press, 2001.
-
(2001)
Diagnosis and Management of Pituitary Tumours
, pp. 295-316
-
-
Quabbe, H.-J.1
Plockinger, U.2
-
109
-
-
84995867100
-
Hypopituitarism beginning in infancy: The Alton Giant
-
Behrens LH & Barr DP. Hypopituitarism beginning in infancy: The Alton Giant. Endocrinology 1932; 16: 120.
-
(1932)
Endocrinology
, vol.16
, pp. 120
-
-
Behrens, L.H.1
Barr, D.P.2
-
111
-
-
0027402350
-
Congenital gigantism due to growth hormone-releasing hormone excess and pituitary hyperplasia with adenomatous transformation
-
Zimmerman D, Young WF Jr, Ebersold MJ et al. Congenital gigantism due to growth hormone-releasing hormone excess and pituitary hyperplasia with adenomatous transformation. Journal of Clinical Endocrinology and Metabolism 1993; 76: 216-222.
-
(1993)
Journal of Clinical Endocrinology and Metabolism
, vol.76
, pp. 216-222
-
-
Zimmerman, D.1
Young W.F., Jr.2
Ebersold, M.J.3
-
112
-
-
0034453781
-
Isolated familial somatotropinomas: Establishment of linkage to chromosome 11q13-1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12
-
Gadelha MR, Une KN, Rohde K et al. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13-1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12. Journal of Clinical Endocrinology and Metabolism 2000; 85: 707-714.
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, pp. 707-714
-
-
Gadelha, M.R.1
Une, K.N.2
Rohde, K.3
-
113
-
-
0035217709
-
Reference values for IGF-I throughout childhood and adolescence: A model that accounts simultaneously for the effect of gender, age, and puberty
-
Lofqvist C, Andersson E, Gelander L et al. Reference values for IGF-I throughout childhood and adolescence: a model that accounts simultaneously for the effect of gender, age, and puberty. Journal of Clinical Endocrinology and Metabolism 2001; 86: 5870-5876.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 5870-5876
-
-
Lofqvist, C.1
Andersson, E.2
Gelander, L.3
-
114
-
-
0029121073
-
Serum levels of insulin-like growth factor (IGF)-binding protein-3 (IGFBP-3) in healthy infants, children, and adolescents: The relation to IGF-I, IGF-II, IGFBP-1, IGFBP-2, age, sex, body mass index, and pubertal maturation
-
Juul A, Dalgaard P, Blum WF et al. Serum levels of insulin-like growth factor (IGF)-binding protein-3 (IGFBP-3) in healthy infants, children, and adolescents: the relation to IGF-I, IGF-II, IGFBP-1, IGFBP-2, age, sex, body mass index, and pubertal maturation. Journal of Clinical Endocrinology and Metabolism 1995; 80: 2534-2542.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 2534-2542
-
-
Juul, A.1
Dalgaard, P.2
Blum, W.F.3
-
115
-
-
0032890679
-
Suppression of growth hormone by oral glucose in the evaluation of tall stature
-
Holl RW, Bucher P, Sorgo W et al. Suppression of growth hormone by oral glucose in the evaluation of tall stature. Hormone Research 1999; 51: 20-24.
-
(1999)
Hormone Research
, vol.51
, pp. 20-24
-
-
Holl, R.W.1
Bucher, P.2
Sorgo, W.3
-
116
-
-
0026689386
-
Pituitary gigantism
-
Lu PW, Silink M, Johnston I, Cowell CT & Jimenez M. Pituitary gigantism. Archives of Disease in Childhood 1992; 67: 1039-1041.
-
(1992)
Archives of Disease in Childhood
, vol.67
, pp. 1039-1041
-
-
Lu, P.W.1
Silink, M.2
Johnston, I.3
Cowell, C.T.4
Jimenez, M.5
-
118
-
-
0030797569
-
Effect of testosterone and estradiol in a man with aromatase deficiency
-
Carani C, Qin K, Simoni M et al. Effect of testosterone and estradiol in a man with aromatase deficiency. New England Journal of Medicine 1997; 337: 91-95.
-
(1997)
New England Journal of Medicine
, vol.337
, pp. 91-95
-
-
Carani, C.1
Qin, K.2
Simoni, M.3
-
120
-
-
0016588841
-
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities
-
Hamerton JL, Canning N, Ray M & Smith S. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clinical Genetics 1975; 8: 223-243.
-
(1975)
Clinical Genetics
, vol.8
, pp. 223-243
-
-
Hamerton, J.L.1
Canning, N.2
Ray, M.3
Smith, S.4
-
122
-
-
0025551161
-
Edinburgh study of growth and development of children with sex chromosome abnormalities. IV
-
Ratcliffe SG, Butler GE & Jones M. Edinburgh study of growth and development of children with sex chromosome abnormalities. IV. Birth Defects Original Article Series 1990; 26: 1-44.
-
(1990)
Birth Defects Original Article Series
, vol.26
, pp. 1-44
-
-
Ratcliffe, S.G.1
Butler, G.E.2
Jones, M.3
-
124
-
-
0020355575
-
Growth and development of children with X and Y chromosome aneuploidy from infancy to pubertal age: The Toronto study
-
Stewart DA, Bailey JD, Netley CT et al. Growth and development of children with X and Y chromosome aneuploidy from infancy to pubertal age: the Toronto study. Birth Defects Original Article Series 1982; 18: 99-154.
-
(1982)
Birth Defects Original Article Series
, vol.18
, pp. 99-154
-
-
Stewart, D.A.1
Bailey, J.D.2
Netley, C.T.3
-
126
-
-
0015435391
-
Pathologic testicular findings in Klinefelter's syndrome 47,XXY vs 46,XY-47,XXY
-
Gordon DL, Krmpotic E, Thomas W et al. Pathologic testicular findings in Klinefelter's syndrome 47,XXY vs 46,XY-47,XXY. Archives of Internal Medicine 1972; 130: 726-729.
-
(1972)
Archives of Internal Medicine
, vol.130
, pp. 726-729
-
-
Gordon, D.L.1
Krmpotic, E.2
Thomas, W.3
-
127
-
-
0035652398
-
Outcome of ICSI using fresh and cryopreserved-thawed testicular spermatozoa in patients with non-mosaic Klinefelter's syndrome
-
Friedler S, Raziel A, Strassburger D et al. Outcome of ICSI using fresh and cryopreserved-thawed testicular spermatozoa in patients with non-mosaic Klinefelter's syndrome. Human Reproduction 2001; 16: 2616-2620.
-
(2001)
Human Reproduction
, vol.16
, pp. 2616-2620
-
-
Friedler, S.1
Raziel, A.2
Strassburger, D.3
-
128
-
-
0034758599
-
Birth of two infants with normal karyotype after intracytoplasmic injection of sperm obtained by testicular extraction from two men with nonmosaic. Klinefelter's syndrome
-
Poulakis V, Witzsch U, Diehl W et al. Birth of two infants with normal karyotype after intracytoplasmic injection of sperm obtained by testicular extraction from two men with nonmosaic. Klinefelter's syndrome. Fertility and Sterility 2001; 76: 1060-1062.
-
(2001)
Fertility and Sterility
, vol.76
, pp. 1060-1062
-
-
Poulakis, V.1
Witzsch, U.2
Diehl, W.3
-
129
-
-
0034809275
-
Birth of a healthy girl after ICSI with ejaculated spermatozoa from a man with non-mosaic Klinefelter's syndrome
-
Cruger D, Toft B, Agerholm I et al. Birth of a healthy girl after ICSI with ejaculated spermatozoa from a man with non-mosaic Klinefelter's syndrome. Human Reproduction 2001; 16: 1909-1911.
-
(2001)
Human Reproduction
, vol.16
, pp. 1909-1911
-
-
Cruger, D.1
Toft, B.2
Agerholm, I.3
-
133
-
-
0023261248
-
Follow-up 20 years later of 34 Klinefelter males with karyotype 47,XXY and 16 hypogonadal males with karyotype 46,XY
-
Nielsen J & Pelsen B. Follow-up 20 years later of 34 Klinefelter males with karyotype 47,XXY and 16 hypogonadal males with karyotype 46,XY. Human Genetics 1987; 77: 188-192.
-
(1987)
Human Genetics
, vol.77
, pp. 188-192
-
-
Nielsen, J.1
Pelsen, B.2
-
134
-
-
0023746674
-
X-chromosome polysomy in the male. The Leuven experience 1966-1987
-
Kleczkowska A, Fryns JP & Van den BH. X-chromosome polysomy in the male. The Leuven experience 1966-1987. Human Genetics 1988; 80: 16-22.
-
(1988)
Human Genetics
, vol.80
, pp. 16-22
-
-
Kleczkowska, A.1
Fryns, J.P.2
Van Den, B.H.3
-
135
-
-
0023922039
-
Follow-up of 30 Klinefelter males treated with testosterone
-
Nielsen J, Pelsen B & Sorensen K. Follow-up of 30 Klinefelter males treated with testosterone. Clinical Genetics 1988; 33: 262-269.
-
(1988)
Clinical Genetics
, vol.33
, pp. 262-269
-
-
Nielsen, J.1
Pelsen, B.2
Sorensen, K.3
-
137
-
-
0025561058
-
Androgen therapy in Klinefelter syndrome during adolescence
-
Winter JS. Androgen therapy in Klinefelter syndrome during adolescence. Birth Defects Original Article Series 1990; 26: 235-245.
-
(1990)
Birth Defects Original Article Series
, vol.26
, pp. 235-245
-
-
Winter, J.S.1
-
138
-
-
0030639722
-
Genetic disorders associated with overgrowth
-
Sotos JF. Genetic disorders associated with overgrowth. Clinical Pediatrics (Philadelphia) 1997; 36: 39-49.
-
(1997)
Clinical Pediatrics (Philadelphia)
, vol.36
, pp. 39-49
-
-
Sotos, J.F.1
-
141
-
-
0025542156
-
Summary of clinical findings in children and young adults with sex chromosome anomalies
-
Robinson A, Bender BG & Linden MG. Summary of clinical findings in children and young adults with sex chromosome anomalies. Birth Defects Original Article Series 1990; 26: 225-228.
-
(1990)
Birth Defects Original Article Series
, vol.26
, pp. 225-228
-
-
Robinson, A.1
Bender, B.G.2
Linden, M.G.3
-
142
-
-
0020443565
-
Summary of clinical findings of children with 47,XXY, 47,XYY, and 47,XXX karyotypes
-
Stewart DA, Netley CT & Park E. Summary of clinical findings of children with 47,XXY, 47,XYY, and 47,XXX karyotypes. Birth Defects Original Article Series 1982; 18: 1-5.
-
(1982)
Birth Defects Original Article Series
, vol.18
, pp. 1-5
-
-
Stewart, D.A.1
Netley, C.T.2
Park, E.3
-
145
-
-
0034927341
-
Quantitative assessment of dural ectasia as a marker for Marfan syndrome
-
Oosterhof T, Groenik M, Hulsman FJ et al. Quantitative assessment of dural ectasia as a marker for Marfan syndrome. Radiology 2001; 220: 514-518.
-
(2001)
Radiology
, vol.220
, pp. 514-518
-
-
Oosterhof, T.1
Groenik, M.2
Hulsman, F.J.3
-
146
-
-
0033757878
-
A comparison of the Berlin and Ghent nosologies and the influence of dural ectasia in the diagnosis of Marfan syndrome
-
Rose PS, Levy HP, Ahn NU et al. A comparison of the Berlin and Ghent nosologies and the influence of dural ectasia in the diagnosis of Marfan syndrome. Genetic Medicine 2000; 2: 278-282.
-
(2000)
Genetic Medicine
, vol.2
, pp. 278-282
-
-
Rose, P.S.1
Levy, H.P.2
Ahn, N.U.3
-
147
-
-
0025801891
-
Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency
-
Buntinx IM, Willems PJ, Spitaels SE et al. Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency. Journal of Medical Genetics 1991; 28: 267-273.
-
(1991)
Journal of Medical Genetics
, vol.28
, pp. 267-273
-
-
Buntinx, I.M.1
Willems, P.J.2
Spitaels, S.E.3
-
148
-
-
0023917651
-
International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986
-
Beighton P, de Paepe A, Danks D et al. International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986. American Journal of Medical Genetics 1988; 29: 581-594.
-
(1988)
American Journal of Medical Genetics
, vol.29
, pp. 581-594
-
-
Beighton, P.1
De Paepe, A.2
Danks, D.3
-
153
-
-
0022625777
-
Surgical treatment of aneurysms of the ascending aorta in the Marfan syndrome. Results of composite-graft repair in 50 patients
-
Gott VL, Pyeritz RE, Magovern GJ Jr et al. Surgical treatment of aneurysms of the ascending aorta in the Marfan syndrome. Results of composite-graft repair in 50 patients. New England Journal of Medicine 1986; 134: 1070-1074.
-
(1986)
New England Journal of Medicine
, vol.314
, pp. 1070-1074
-
-
Gott, V.L.1
Pyeritz, R.E.2
Magovern G.J., Jr.3
-
154
-
-
0033614448
-
Replacement of the aortic root in patients with Marfan's syndrome
-
Gott VL, Greene PS, Alejo DE et al. Replacement of the aortic root in patients with Marfan's syndrome. New England Journal of Medicine 1999; 340: 1307-1313.
-
(1999)
New England Journal of Medicine
, vol.340
, pp. 1307-1313
-
-
Gott, V.L.1
Greene, P.S.2
Alejo, D.E.3
-
155
-
-
0028296142
-
Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome
-
Shores J, Berger KR, Murphy EA & Pyeritz RE. Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome. New England Journal of Medicine 1994; 330: 1335-1341.
-
(1994)
New England Journal of Medicine
, vol.330
, pp. 1335-1341
-
-
Shores, J.1
Berger, K.R.2
Murphy, E.A.3
Pyeritz, R.E.4
-
156
-
-
0015093747
-
Congenital contractural arachnodactyly. A heritable disorder of connective tissue
-
Beals RK & Hecht F. Congenital contractural arachnodactyly. A heritable disorder of connective tissue. Journal of Bone and Joint Surgery (Am) 1971; 53: 987-993.
-
(1971)
Journal of Bone and Joint Surgery (Am)
, vol.53
, pp. 987-993
-
-
Beals, R.K.1
Hecht, F.2
-
157
-
-
18244366671
-
Ten novel FBN2 mutations in congenital contractural arachnodactyly: Delineation of the molecular pathogenesis and clinical phenotype
-
Gupta PA, Putnam EA, Carmical SG et al. Ten novel FBN2 mutations in congenital contractural arachnodactyly: delineation of the molecular pathogenesis and clinical phenotype. Human Mutations 2002; 19: 39-48.
-
(2002)
Human Mutations
, vol.19
, pp. 39-48
-
-
Gupta, P.A.1
Putnam, E.A.2
Carmical, S.G.3
-
158
-
-
0001445647
-
Cerebral gigantism in childhood: A syndrome of excessively rapid growth and acromegalic features and a non-progressive neural disorder
-
Sotos JF, Dodge PR, Muirhead D et al. Cerebral gigantism in childhood: a syndrome of excessively rapid growth and acromegalic features and a non-progressive neural disorder. New England Journal of Medicine 1964; 271: 109-116.
-
(1964)
New England Journal of Medicine
, vol.271
, pp. 109-116
-
-
Sotos, J.F.1
Dodge, P.R.2
Muirhead, D.3
-
159
-
-
0031038991
-
Overgrowth. Section V. Syndromes and other disorders associated with overgrowth
-
Sotos JF. Overgrowth. Section V. Syndromes and other disorders associated with overgrowth. Clinical Pediatrics (Philadelphia) 1997; 36: 89-103.
-
(1997)
Clinical Pediatrics (Philadelphia)
, vol.36
, pp. 89-103
-
-
Sotos, J.F.1
-
160
-
-
0032101633
-
Accelerated linear growth and advanced bone age in Sotos syndrome is not associated with abnormalities of collagen metabolism
-
Rao VH, Buehler BA & Schaefer GB. Accelerated linear growth and advanced bone age in Sotos syndrome is not associated with abnormalities of collagen metabolism. Clinical Biochemistry 1998; 34: 241-249.
-
(1998)
Clinical Biochemistry
, vol.31
, pp. 241-249
-
-
Rao, V.H.1
Buehler, B.A.2
Schaefer, G.B.3
-
161
-
-
0031020714
-
No evidence for uniparental disomy as a common cause of Sotos syndrome
-
Smith M, Fullwood P, Qi Y et al. No evidence for uniparental disomy as a common cause of Sotos syndrome. Journal of Medical Genetics 1997; 34: 10-12.
-
(1997)
Journal of Medical Genetics
, vol.34
, pp. 10-12
-
-
Smith, M.1
Fullwood, P.2
Qi, Y.3
-
163
-
-
0021819990
-
Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases. Analysis of clinical features, growth and plasma somatomedin
-
Wit JM, Beemer FA, Barth PG et al. Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases. Analysis of clinical features, growth and plasma somatomedin. European Journal of Pediatrics 1985; 144: 131-140.
-
(1985)
European Journal of Pediatrics
, vol.144
, pp. 131-140
-
-
Wit, J.M.1
Beemer, F.A.2
Barth, P.G.3
-
166
-
-
0028078759
-
Sotos syndrome: A study of the diagnostic criteria and natural history
-
Cole TR & Hughes HE. Sotos syndrome: a study of the diagnostic criteria and natural history. Journal of Medical Genetics 1994; 31: 20-32.
-
(1994)
Journal of Medical Genetics
, vol.31
, pp. 20-32
-
-
Cole, T.R.1
Hughes, H.E.2
-
172
-
-
0030639722
-
Genetic disorders associated with overgrowth
-
Sotos JF. Genetic disorders associated with overgrowth. Clinical Pediatrics (Philadelphia) 1997; 36: 39-49.
-
(1997)
Clinical Pediatrics (Philadelphia)
, vol.36
, pp. 39-49
-
-
Sotos, J.F.1
-
173
-
-
0034988915
-
Influence of metabolic control on growth in homocystinuria due to cystathionine B-synthase deficiency
-
Topaloglu AK, Sansaricq C & Snyderman SE. Influence of metabolic control on growth in homocystinuria due to cystathionine B-synthase deficiency. Pediatric Research 2001; 49: 796-798.
-
(2001)
Pediatric Research
, vol.49
, pp. 796-798
-
-
Topaloglu, A.K.1
Sansaricq, C.2
Snyderman, S.E.3
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