-
1
-
-
0026350171
-
Pituitary evaluation and growth hormone treatment in Prader-Willi Syndrome
-
Angulo M, Castro-Magana M, Uy J (1991) Pituitary evaluation and growth hormone treatment in Prader-Willi Syndrome. J Pediatr Endocrinol 4:167-173
-
(1991)
J Pediatr Endocrinol
, vol.4
, pp. 167-173
-
-
Angulo, M.1
Castro-Magana, M.2
Uy, J.3
-
2
-
-
0030016685
-
Growth hormone secretion and effects of growth hormone therapy on growth velocity and weight gain in children with Prader-Willi syndrome
-
Angulo M, Castro-Magana M, Mazur B, Canas JA, Vitollo M, Sarrantonio M (1996) Growth hormone secretion and effects of growth hormone therapy on growth velocity and weight gain in children with Prader-Willi syndrome. J Pediatr Endocrinol Metab 9:393-400
-
(1996)
J Pediatr Endocrinol Metab
, vol.9
, pp. 393-400
-
-
Angulo, M.1
Castro-Magana, M.2
Mazur, B.3
Canas, J.A.4
Vitollo, M.5
Sarrantonio, M.6
-
3
-
-
0025165774
-
Physical features of Prader-Willi Syndrome in Neonates
-
Aughton DJ, Cassidy S (1990) Physical features of Prader-Willi Syndrome in Neonates. Am J Dis Child 144:1251-1254
-
(1990)
Am J Dis Child
, vol.144
, pp. 1251-1254
-
-
Aughton, D.J.1
Cassidy, S.2
-
4
-
-
0025248270
-
Normal size of hands and feet in Prader-Willi Syndrome
-
Baroncini A, Forabosco A (1990) Normal size of hands and feet in Prader-Willi Syndrome. Clin Genet 37:283-284
-
(1990)
Clin Genet
, vol.37
, pp. 283-284
-
-
Baroncini, A.1
Forabosco, A.2
-
5
-
-
0030443130
-
GH secretion in Prader-Labhard-Willi syndrome: Somatotrope responsiveness to GHRH is enhanced by arginine but not by pyridostigmine
-
Beccaria L, Bosio L, Sanzari A, Aimaretti G, Ghigo E, Chiumello G (1996) GH secretion in Prader-Labhard-Willi syndrome: somatotrope responsiveness to GHRH is enhanced by arginine but not by pyridostigmine. J Pediatr Endocrinol Metab 9:577-583
-
(1996)
J Pediatr Endocrinol Metab
, vol.9
, pp. 577-583
-
-
Beccaria, L.1
Bosio, L.2
Sanzari, A.3
Aimaretti, G.4
Ghigo, E.5
Chiumello, G.6
-
6
-
-
0025666837
-
Psychological profile and behavioural characteristics in 12 patients with Prader-Willi Syndrome
-
Borghgraef M, Fryns J-P, Van de Berghe H (1990) Psychological profile and behavioural characteristics in 12 patients with Prader-Willi Syndrome. Genet Couns 38:141-150
-
(1990)
Genet Couns
, vol.38
, pp. 141-150
-
-
Borghgraef, M.1
Fryns, J.-P.2
Van De Berghe, H.3
-
7
-
-
0025674530
-
Normative standards and comparison of anthropometric data of white and black newborn infants
-
Brandt JM, Allen GA, Haynes JL, Butler MG (1990) Normative standards and comparison of anthropometric data of white and black newborn infants. Dysmorph Clin Genet 4:121-137
-
(1990)
Dysmorph Clin Genet
, vol.4
, pp. 121-137
-
-
Brandt, J.M.1
Allen, G.A.2
Haynes, J.L.3
Butler, M.G.4
-
8
-
-
15644376168
-
Prader-Labhart-Willi syndrome: An overview
-
Bray GA, Wilson WG (1986) Prader-Labhart-Willi syndrome: an overview. Growth, Genet Horm 2: 1-5
-
(1986)
Growth, Genet Horm
, vol.2
, pp. 1-5
-
-
Bray, G.A.1
Wilson, W.G.2
-
9
-
-
0020540604
-
The Prader-Willi syndrome: A study of 40 patients and a review of the literature
-
Bray GA, Dahms WT, Swerdloff RS, Fiser RH, Atkinson RL, Carrel RE (1983) The Prader-Willi syndrome: a study of 40 patients and a review of the literature. Medicine 62:59-80
-
(1983)
Medicine
, vol.62
, pp. 59-80
-
-
Bray, G.A.1
Dahms, W.T.2
Swerdloff, R.S.3
Fiser, R.H.4
Atkinson, R.L.5
Carrel, R.E.6
-
10
-
-
0022879807
-
An anthropometric study of 38 individuals with Prader-Labhart-Willi Syndrome
-
Butler MG, Meaney FJ (1987) An anthropometric study of 38 individuals with Prader-Labhart-Willi Syndrome. Am J Med Genet 26:445-455
-
(1987)
Am J Med Genet
, vol.26
, pp. 445-455
-
-
Butler, M.G.1
Meaney, F.J.2
-
11
-
-
0025997680
-
Standards for selected anthropometric measurements in Prader-Willi Syndrome
-
Butler MG, Meaney FJ (1991) Standards for selected anthropometric measurements in Prader-Willi Syndrome. Pediatrics 88:853-860
-
(1991)
Pediatrics
, vol.88
, pp. 853-860
-
-
Butler, M.G.1
Meaney, F.J.2
-
12
-
-
0022462350
-
Clinical and cytogenetic survey of 39 individuals with Prader-Willi Syndrome
-
Butler MG, Meaney FJ, Palmer CG (1986) Clinical and cytogenetic survey of 39 individuals with Prader-Willi Syndrome. Am J Med Genet 23:793-809
-
(1986)
Am J Med Genet
, vol.23
, pp. 793-809
-
-
Butler, M.G.1
Meaney, F.J.2
Palmer, C.G.3
-
13
-
-
0023796516
-
The use of skinfold measurements to judge obesity during the early phase of Prader-Labhart-Willi syndrome
-
Butler MG, Butler RI, Meany FJ (1988) The use of skinfold measurements to judge obesity during the early phase of Prader-Labhart-Willi syndrome. Int J Obes 12:417-422
-
(1988)
Int J Obes
, vol.12
, pp. 417-422
-
-
Butler, M.G.1
Butler, R.I.2
Meany, F.J.3
-
14
-
-
0025957350
-
Anthropometric study with emphasis on hand and foot measurements in Prader-Willi Syndrome: Sex, age and chromosome effects
-
Butler MG, Haynes JL, Meaney FJ (1991a) Anthropometric study with emphasis on hand and foot measurements in Prader-Willi Syndrome: sex, age and chromosome effects. Clin Genet 39:39-47
-
(1991)
Clin Genet
, vol.39
, pp. 39-47
-
-
Butler, M.G.1
Haynes, J.L.2
Meaney, F.J.3
-
15
-
-
0026058809
-
Studio endocrino nella sindrome di Prader-Willi. A proposito di 5 casi
-
Calisti I, Giannessi N, Saggese G (1991) Studio endocrino nella sindrome di Prader-Willi. A proposito di 5 casi. Minerva Pediatr 43:587-593
-
(1991)
Minerva Pediatr
, vol.43
, pp. 587-593
-
-
Calisti, I.1
Giannessi, N.2
Saggese, G.3
-
16
-
-
0027270979
-
Growth hormone (GH) response to combined pyridostigmine and GH-releasing hormone administration in patients with Prader-Labhart-Willi Syndrome
-
Cappa M, Grossi A, Borrelli P, Ghigo E, Bellone J, Benedetti S, Carta D, Loche S (1993) Growth hormone (GH) response to combined pyridostigmine and GH-releasing hormone administration in patients with Prader-Labhart-Willi Syndrome. Horm Res 39:51-55
-
(1993)
Horm Res
, vol.39
, pp. 51-55
-
-
Cappa, M.1
Grossi, A.2
Borrelli, P.3
Ghigo, E.4
Bellone, J.5
Benedetti, S.6
Carta, D.7
Loche, S.8
-
17
-
-
0025910619
-
Prader-Willi syndrome and Robertsonian translocations involving chromosome 15
-
Casamassima AC, Shapiro L, Wilmot PL, Smith KB (1991) Prader-Willi syndrome and Robertsonian translocations involving chromosome 15. Clin Genet 39:294-297
-
(1991)
Clin Genet
, vol.39
, pp. 294-297
-
-
Casamassima, A.C.1
Shapiro, L.2
Wilmot, P.L.3
Smith, K.B.4
-
18
-
-
0031015938
-
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15
-
Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S (1997) Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15. Am J Med Genet 68:433-40
-
(1997)
Am J Med Genet
, vol.68
, pp. 433-440
-
-
Cassidy, S.B.1
Forsythe, M.2
Heeger, S.3
Nicholls, R.D.4
Schork, N.5
Benn, P.6
Schwartz, S.7
-
19
-
-
0024516927
-
Perinatal and first year follow-up of patients with Prader-Willi Syndrome: Normal size of hands and feet
-
Chitayat D, Davis EB, McGillivray BC, Hall H u.JG (1989) Perinatal and first year follow-up of patients with Prader-Willi Syndrome: normal size of hands and feet. Clin Genet 35:161-166
-
(1989)
Clin Genet
, vol.35
, pp. 161-166
-
-
Chitayat, D.1
Davis, E.B.2
McGillivray, B.C.3
Hall, HuJ.G.4
-
20
-
-
0024204903
-
Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: A new X-linked mental retardation syndrome
-
Chudley AE, Lowry RB, Hoar DI (1988) Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome. Am J Med Genet 31:741-751
-
(1988)
Am J Med Genet
, vol.31
, pp. 741-751
-
-
Chudley, A.E.1
Lowry, R.B.2
Hoar, D.I.3
-
22
-
-
0002978383
-
Weight-stature indices to measure underweight, overweight, and obesity
-
Himes JH (ed) Wiley & Sons, New York
-
Cole TJ (1991) Weight-stature indices to measure underweight, overweight, and obesity. In: Himes JH (ed) Anthropometric assessment of nutritional status. Wiley & Sons, New York, pp 83-112
-
(1991)
Anthropometric Assessment of Nutritional Status
, pp. 83-112
-
-
Cole, T.J.1
-
23
-
-
0027252501
-
Effects of growth hormone in Prader-Willi Syndrome
-
Connor EL, Rosenbloom A (1993) Effects of growth hormone in Prader-Willi Syndrome (Editorial). Clin Pediatr 32:296-297
-
(1993)
Clin Pediatr
, vol.32
, pp. 296-297
-
-
Connor, E.L.1
Rosenbloom, A.2
-
25
-
-
0026782059
-
Assessment of body composition in the Prader-Willi syndrome using bioelectrical impedance
-
Davies PS, Joughin C (1992) Assessment of body composition in the Prader-Willi syndrome using bioelectrical impedance. Am J Med Genet 44:75-78
-
(1992)
Am J Med Genet
, vol.44
, pp. 75-78
-
-
Davies, P.S.1
Joughin, C.2
-
26
-
-
0028220882
-
The Prader-Willi syndrome
-
Donaldson MD, Chu CE, Cooke A, Wilson A, Greene SA, Stephenson JB (1994) The Prader-Willi syndrome. Arch Dis Child 70:58-63
-
(1994)
Arch Dis Child
, vol.70
, pp. 58-63
-
-
Donaldson, M.D.1
Chu, C.E.2
Cooke, A.3
Wilson, A.4
Greene, S.A.5
Stephenson, J.B.6
-
27
-
-
0021026879
-
Investigations on patients with the Prader-Labhart-Willi-Syndrome
-
Fesseler WH, Bierich JR (1983) Investigations on patients with the Prader-Labhart-Willi-Syndrome. Monatsschr Kinderheilkd 131:844-847
-
(1983)
Monatsschr Kinderheilkd
, vol.131
, pp. 844-847
-
-
Fesseler, W.H.1
Bierich, J.R.2
-
28
-
-
0022609038
-
Coexistence of Prader-Willi Syndrome, congenital ectropion uveae with glaucoma, and factor XI deficiency
-
Futterweit W, Ritch R, Teekhasaenee C, Nelson ES (1986) Coexistence of Prader-Willi Syndrome, congenital ectropion uveae with glaucoma, and factor XI deficiency. JAMA 255:3280-3282
-
(1986)
JAMA
, vol.255
, pp. 3280-3282
-
-
Futterweit, W.1
Ritch, R.2
Teekhasaenee, C.3
Nelson, E.S.4
-
29
-
-
0028900374
-
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome
-
Gillessen-Kaesbach G, Gross G, Kaya-Westerloh S, Passarge E, Horsthemke B (1995) DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome. J Med Genet 32:88-92
-
(1995)
J Med Genet
, vol.32
, pp. 88-92
-
-
Gillessen-Kaesbach, G.1
Gross, G.2
Kaya-Westerloh, S.3
Passarge, E.4
Horsthemke, B.5
-
30
-
-
0028892266
-
Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome
-
Gillessen-Kaesbach G, Robinson W, Lohmann D, Kaya-Westerloh S, Passarge E, Horsthemke B (1995a) Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome. Hum Genet 96:638-643
-
(1995)
Hum Genet
, vol.96
, pp. 638-643
-
-
Gillessen-Kaesbach, G.1
Robinson, W.2
Lohmann, D.3
Kaya-Westerloh, S.4
Passarge, E.5
Horsthemke, B.6
-
31
-
-
0023135272
-
Adults with Prader-Willi syndrome: A survey or 232 cases
-
Greenswag LR (1987) Adults with Prader-Willi syndrome: a survey or 232 cases. Dev Med Child Neurol 29:145-152
-
(1987)
Dev Med Child Neurol
, vol.29
, pp. 145-152
-
-
Greenswag, L.R.1
-
32
-
-
0026042457
-
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi Syndrome
-
Gregory CA, Schwartz J, Kirkilionis AJ, Rudi N, Hamerton JL (1991) Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi Syndrome. Hum Genet 88:42-48
-
(1991)
Hum Genet
, vol.88
, pp. 42-48
-
-
Gregory, C.A.1
Schwartz, J.2
Kirkilionis, A.J.3
Rudi, N.4
Hamerton, J.L.5
-
34
-
-
0015387610
-
Prader-Willi Syndrome. A resume of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence
-
Hall BD, Smith DW (1972) Prader-Willi Syndrome. A resume of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence. J Pediatr 81:286-293
-
(1972)
J Pediatr
, vol.81
, pp. 286-293
-
-
Hall, B.D.1
Smith, D.W.2
-
35
-
-
0027399648
-
Tall stature: An atypical phenotype in Prader-Willi Syndrome
-
Harty JR, Hollowell JG, Sieg KG (1993) Tall stature: An atypical phenotype in Prader-Willi Syndrome. Clin Pediatr 32:179-180
-
(1993)
Clin Pediatr
, vol.32
, pp. 179-180
-
-
Harty, J.R.1
Hollowell, J.G.2
Sieg, K.G.3
-
36
-
-
0008616013
-
Statistics of growth standards
-
Falkner N, Tanner JM (eds) Plenum Press, New York
-
Healy MJR (1986) Statistics of growth standards. In: Falkner N, Tanner JM (eds) Human Growth, a comprehensive treatise (2nd edition). Plenum Press, New York, pp 226-242
-
(1986)
Human Growth, a Comprehensive Treatise (2nd Edition)
, pp. 226-242
-
-
Healy, M.J.R.1
-
37
-
-
0028144688
-
Guidelines for overweight in adolescent preventive services: Recommendations from an expert committee
-
Himes JH, Dietz WH (1994) Guidelines for overweight in adolescent preventive services: recommendations from an expert committee. Am J Clin Nutr 59:307-316
-
(1994)
Am J Clin Nutr
, vol.59
, pp. 307-316
-
-
Himes, J.H.1
Dietz, W.H.2
-
38
-
-
0002383429
-
The diagnosis of Prader-Willi syndrome
-
Holm VA, Sulzbacher S, Pipes PL (eds) University Park Press Baltimore
-
Holm VA (1981) The diagnosis of Prader-Willi syndrome. In: Holm VA, Sulzbacher S, Pipes PL (eds) The Prader-Willi Syndrome. University Park Press Baltimore, pp 27-36
-
(1981)
The Prader-Willi Syndrome
, pp. 27-36
-
-
Holm, V.A.1
-
40
-
-
0027476242
-
Prader-Willi Syndrome: Consensus diagnostic criteria
-
Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F (1993) Prader-Willi Syndrome: Consensus diagnostic criteria. Pediatrics 91:398-402
-
(1993)
Pediatrics
, vol.91
, pp. 398-402
-
-
Holm, V.A.1
Cassidy, S.B.2
Butler, M.G.3
Hanchett, J.M.4
Greenswag, L.R.5
Whitman, B.Y.6
Greenberg, F.7
-
41
-
-
0025342495
-
Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi Syndrome
-
Hoo J-J, Chao MC, Morgan S u.A (1990) Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi Syndrome. Clin Genet 37:161-166
-
(1990)
Clin Genet
, vol.37
, pp. 161-166
-
-
Hoo, J.-J.1
Chao, M.C.2
Morgan, Su.A.3
-
42
-
-
0026329191
-
Hand and foot length in Prader-Willi Syndrome
-
Hudgins L, Cassidy SB (1991) Hand and foot length in Prader-Willi Syndrome. Am J Med Genet 41:5-9
-
(1991)
Am J Med Genet
, vol.41
, pp. 5-9
-
-
Hudgins, L.1
Cassidy, S.B.2
-
44
-
-
0018069773
-
Pubertal development in the Prader-Labhart-Willi syndrome
-
Kauli R, Prager-Lewin R, Laron Z (1978) Pubertal development in the Prader-Labhart-Willi syndrome. Acta Paediatr Scand 67:763-767
-
(1978)
Acta Paediatr Scand
, vol.67
, pp. 763-767
-
-
Kauli, R.1
Prager-Lewin, R.2
Laron, Z.3
-
46
-
-
0026924041
-
Prader-Willi Syndrome associated with chromosomal aberration: Report of a case
-
Kokura K, Shima H, Mori Y, Ikoma F, Sakamoto H, Furuyama J (1992) Prader-Willi Syndrome associated with chromosomal aberration: report of a case. Acta Urol Jpn 38:1079-1082
-
(1992)
Acta Urol Jpn
, vol.38
, pp. 1079-1082
-
-
Kokura, K.1
Shima, H.2
Mori, Y.3
Ikoma, F.4
Sakamoto, H.5
Furuyama, J.6
-
48
-
-
0019166386
-
Evaluation of perinatal growth. Presentation of combined intra- and extrauterine growth standards for weight, length and head circumference
-
Largo RH, Wälli R, Duc G, Fanconi A, Prader A (1980) Evaluation of perinatal growth. Presentation of combined intra- and extrauterine growth standards for weight, length and head circumference. Helv Paediatr Acta 35:419-436
-
(1980)
Helv Paediatr Acta
, vol.35
, pp. 419-436
-
-
Largo, R.H.1
Wälli, R.2
Duc, G.3
Fanconi, A.4
Prader, A.5
-
49
-
-
0025007680
-
Prenatal diagnosis of del(15)(q11q13)
-
Le Bris-Quillevere MJ, Riviere D, Pluchon-Riviere E, Chabaud JJ, Parent P, Volant A, Boog G (1990) Prenatal diagnosis of del(15)(q11q13). Prenat Diagn 10:405-411
-
(1990)
Prenat Diagn
, vol.10
, pp. 405-411
-
-
Le Bris-Quillevere, M.J.1
Riviere, D.2
Pluchon-Riviere, E.3
Chabaud, J.J.4
Parent, P.5
Volant, A.6
Boog, G.7
-
50
-
-
0019377986
-
Deletions of chromosome 15 as a cause of the Prader-Willi Syndrome
-
Ledbetter DH, Riccardi VM, Airhart SD, Strobel RJ, Keenan BS, Crawford JD (1981) Deletions of chromosome 15 as a cause of the Prader-Willi Syndrome. N Engl J Med 304:325-329
-
(1981)
N Engl J Med
, vol.304
, pp. 325-329
-
-
Ledbetter, D.H.1
Riccardi, V.M.2
Airhart, S.D.3
Strobel, R.J.4
Keenan, B.S.5
Crawford, J.D.6
-
53
-
-
0025891980
-
Anaesthesia and the Prader-Willi Syndrome
-
Mackenzie JW (1991) Anaesthesia and the Prader-Willi Syndrome. J R Soc Med 84:239
-
(1991)
J R Soc Med
, vol.84
, pp. 239
-
-
Mackenzie, J.W.1
-
55
-
-
0020512319
-
Prader-Willi Syndrome and chromosome 15
-
Mattei JF, Mattei MG, Giraud F (1983) Prader-Willi Syndrome and chromosome 15. Hum Genet 64:356-362
-
(1983)
Hum Genet
, vol.64
, pp. 356-362
-
-
Mattei, J.F.1
Mattei, M.G.2
Giraud, F.3
-
56
-
-
0021324098
-
Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis
-
Mattei MG, Souiah N, Mattei JF (1984) Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis. Hum Genet 66:313-334
-
(1984)
Hum Genet
, vol.66
, pp. 313-334
-
-
Mattei, M.G.1
Souiah, N.2
Mattei, J.F.3
-
57
-
-
0026607114
-
Unique karyotypes in two patients with Prader-Willi Syndrome
-
Narahara K, Hiramoto K, Murakami M, Miyake S, Tsuji K, Yokoyama Y, Namba H, Ninomiya S, Murakami R, Seino Y (1992) Unique karyotypes in two patients with Prader-Willi Syndrome. Am J Med Genet 42:671-677
-
(1992)
Am J Med Genet
, vol.42
, pp. 671-677
-
-
Narahara, K.1
Hiramoto, K.2
Murakami, M.3
Miyake, S.4
Tsuji, K.5
Yokoyama, Y.6
Namba, H.7
Ninomiya, S.8
Murakami, R.9
Seino, Y.10
-
58
-
-
4243462581
-
Selected body measurements of children 6-11 years, United States
-
Washington, DC: US Public Health Service US Dept of Health, Education, and Welfare publication (HSM) 11
-
National Center for Health Statistics. Selected body measurements of children 6-11 years, United States. In: Vital and Health Statistics. Washington, DC: US Public Health Service (1973) US Dept of Health, Education, and Welfare publication (HSM) 11; 123:73-1605
-
(1973)
Vital and Health Statistics
, vol.123
, pp. 73-1605
-
-
-
59
-
-
0027474137
-
Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndrome
-
Nicholls RD (1993) Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndrome. Am J Med Genet 46:16-25
-
(1993)
Am J Med Genet
, vol.46
, pp. 16-25
-
-
Nicholls, R.D.1
-
60
-
-
0002383429
-
Physical growth in Prader-Willi syndrome
-
Holm VA, Sulzbacher S, Pipes PL (eds) University Park Press, Baltimore, chapter 21
-
Nugent JK, Holm VA (1981) Physical growth in Prader-Willi syndrome. In: Holm VA, Sulzbacher S, Pipes PL (eds) Prader-Willi Syndrome. University Park Press, Baltimore, chapter 21
-
(1981)
Prader-Willi Syndrome
-
-
Nugent, J.K.1
Holm, V.A.2
-
61
-
-
0026779152
-
Prader-Willi Syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13
-
Örstavìk KH, Tangsrud SE, Kill R, Hansteen I-L, Steen-Johnsen J, Cassidy SB, Martony A, Anvret M, Tommerup N (1992) Prader-Willi Syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13. Am J Med Genet 44:534-538
-
(1992)
Am J Med Genet
, vol.44
, pp. 534-538
-
-
Örstavìk, K.H.1
Tangsrud, S.E.2
Kill, R.3
Hansteen, I.-L.4
Steen-Johnsen, J.5
Cassidy, S.B.6
Martony, A.7
Anvret, M.8
Tommerup, N.9
-
62
-
-
0015623926
-
Weight control of children with Prader-Willi Syndrome
-
Pipes PL, Holm VA (1973) Weight control of children with Prader-Willi Syndrome. J Am Diet Assoc 62:520-524
-
(1973)
J Am Diet Assoc
, vol.62
, pp. 520-524
-
-
Pipes, P.L.1
Holm, V.A.2
-
63
-
-
0000927260
-
Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter
-
Prader A, Labhart A, Willi H (1956) Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz Med Wochenschr 86:1260-1261
-
(1956)
Schweiz Med Wochenschr
, vol.86
, pp. 1260-1261
-
-
Prader, A.1
Labhart, A.2
Willi, H.3
-
65
-
-
0026541093
-
Deletion of chromosome 15pter-q11.2 due to t(Y;15) in a boy with Prader-Willi Syndrome
-
Qumsiyeh MB, Dalton JD, Gordon PL, Wilroy RS, Tharapel AT (1992) Deletion of chromosome 15pter-q11.2 due to t(Y;15) in a boy with Prader-Willi Syndrome. Am J Med Genet 42:109 111
-
(1992)
Am J Med Genet
, vol.42
, pp. 109111
-
-
Qumsiyeh, M.B.1
Dalton, J.D.2
Gordon, P.L.3
Wilroy, R.S.4
Tharapel, A.T.5
-
66
-
-
0024345360
-
Disease-specific growth charts do we need them?
-
Ranke MB (1989) Disease-specific growth charts do we need them? Acta Paediatr Scand [Suppl] 356:17-25
-
(1989)
Acta Paediatr Scand [Suppl]
, vol.356
, pp. 17-25
-
-
Ranke, M.B.1
-
67
-
-
0020264431
-
Adiposity indices in children
-
Rolland-Cachera MF, Sempé M, Guilloud-Bataille M, Patois E, Péquignot-Guggenbuhl F, Fautrad V (1982) Adiposity indices in children. Am J Clin Nutr 36:178-184
-
(1982)
Am J Clin Nutr
, vol.36
, pp. 178-184
-
-
Rolland-Cachera, M.F.1
Sempé, M.2
Guilloud-Bataille, M.3
Patois, E.4
Péquignot-Guggenbuhl, F.5
Fautrad, V.6
-
68
-
-
0027294643
-
Effects of growth hormone in Prader-Willi Syndrome
-
Ruvalcaba HA, Holm VA (1993) Effects of growth hormone in Prader-Willi Syndrome. Clin Pediatr 32:292-295
-
(1993)
Clin Pediatr
, vol.32
, pp. 292-295
-
-
Ruvalcaba, H.A.1
Holm, V.A.2
-
69
-
-
0031055875
-
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation
-
Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD (1997) Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation. Am J Med Genet 68:195-206
-
(1997)
Am J Med Genet
, vol.68
, pp. 195-206
-
-
Saitoh, S.1
Buiting, K.2
Cassidy, S.B.3
Conroy, J.M.4
Driscoll, D.J.5
Gabriel, J.M.6
Gillessen-Kaesbach, G.7
Glenn, C.C.8
Greenswag, L.R.9
Horsthemke, B.10
Kondo, I.11
Kuwajima, K.12
Niikawa, N.13
Rogan, P.K.14
Schwartz, S.15
Seip, J.16
Williams, C.A.17
Nicholls, R.D.18
-
70
-
-
0025337646
-
Cephalometric analysis of the Prader-Willi Syndrome
-
Schaedel R, Poole AE, Cassidy SB (1990) Cephalometric analysis of the Prader-Willi Syndrome. Am J Med Genet 36:484-487
-
(1990)
Am J Med Genet
, vol.36
, pp. 484-487
-
-
Schaedel, R.1
Poole, A.E.2
Cassidy, S.B.3
-
71
-
-
0023835578
-
Energy expenditure and body composition in Prader-Willi syndrome
-
Schoeller DA, Levitsky LL, Bandini LG, Dietz WW, Walczak A (1988) Energy expenditure and body composition in Prader-Willi syndrome. Metabolism 37:115-120
-
(1988)
Metabolism
, vol.37
, pp. 115-120
-
-
Schoeller, D.A.1
Levitsky, L.L.2
Bandini, L.G.3
Dietz, W.W.4
Walczak, A.5
-
72
-
-
0026566594
-
Prader-Willi Syndrome and Angelman Syndrome in cousins from a family with a translocation between chromosome 6 and 15
-
Smeets DFCM, Hamel BCJ, Nelen MR, Smeets HJM, Bollen JHM, Smits APT, Ropers H-H, Van Oost BA (1992) Prader-Willi Syndrome and Angelman Syndrome in cousins from a family with a translocation between chromosome 6 and 15. N Engl J Med 326:807-811
-
(1992)
N Engl J Med
, vol.326
, pp. 807-811
-
-
Smeets, D.F.C.M.1
Hamel, B.C.J.2
Nelen, M.R.3
Smeets, H.J.M.4
Bollen, J.H.M.5
Smits, A.P.T.6
Ropers, H.-H.7
Van Oost, B.A.8
-
73
-
-
0025736695
-
A de novo unbalanced reciprocal translocation identified as paternal in origin in Prader-Willi Syndrome
-
Smith A, Lindeman R, Volpato F, Kearney A, White S, Haan E, Trent RJ (1991) A de novo unbalanced reciprocal translocation identified as paternal in origin in Prader-Willi Syndrome. Hum Genet 86:534-536
-
(1991)
Hum Genet
, vol.86
, pp. 534-536
-
-
Smith, A.1
Lindeman, R.2
Volpato, F.3
Kearney, A.4
White, S.5
Haan, E.6
Trent, R.J.7
-
74
-
-
0022978730
-
High-resolution cytogenetic studies in patients with Prader-Willi Syndrome
-
Takano T, Nakagome Y, Nagafuchi S, Tanaka F, Nakamura Y, Nagano T, Tanae A, Hibi I (1986) High-resolution cytogenetic studies in patients with Prader-Willi Syndrome. Clin Genet 30:241-248
-
(1986)
Clin Genet
, vol.30
, pp. 241-248
-
-
Takano, T.1
Nakagome, Y.2
Nagafuchi, S.3
Tanaka, F.4
Nakamura, Y.5
Nagano, T.6
Tanae, A.7
Hibi, I.8
-
75
-
-
0002820557
-
The assessment of growth and development in children
-
Tanner JM (1952) The assessment of growth and development in children. Arch Dis Child 27:10-33
-
(1952)
Arch Dis Child
, vol.27
, pp. 10-33
-
-
Tanner, J.M.1
-
76
-
-
0021184967
-
Precocious puberty in a male with Prader-Labhart-Willi syndrome
-
Vanelli M, Bernasconi S, Caronna N, Viridis R, Terzi C, Giovanelli G (1984) Precocious puberty in a male with Prader-Labhart-Willi syndrome. Helv Paediatr Acta 39:373-377
-
(1984)
Helv Paediatr Acta
, vol.39
, pp. 373-377
-
-
Vanelli, M.1
Bernasconi, S.2
Caronna, N.3
Viridis, R.4
Terzi, C.5
Giovanelli, G.6
-
77
-
-
0023902405
-
Growth and development in simple obesity
-
Vignolo M, Naselli A, Di-Battista E, Mostert M, Aicardi G (1988) Growth and development in simple obesity. Eur J Pediatr 147(3):242-244
-
(1988)
Eur J Pediatr
, vol.147
, Issue.3
, pp. 242-244
-
-
Vignolo, M.1
Naselli, A.2
Di-Battista, E.3
Mostert, M.4
Aicardi, G.5
-
78
-
-
0028917529
-
A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome
-
Webb T, Clarke D, Hardy CA, Kilpatrick MW, Corbett J, Dahlitz M (1995) A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome. J Med Genet 32:181-185
-
(1995)
J Med Genet
, vol.32
, pp. 181-185
-
-
Webb, T.1
Clarke, D.2
Hardy, C.A.3
Kilpatrick, M.W.4
Corbett, J.5
Dahlitz, M.6
-
79
-
-
0028843182
-
Body mass index centile charts to assess fatness of British children
-
White EM, Wilson AC, Greene SA, McCowan C, Thomas GE, Cairns AY, Ricketts IW (1995) Body mass index centile charts to assess fatness of British children. Arch Dis Child 72:38-41
-
(1995)
Arch Dis Child
, vol.72
, pp. 38-41
-
-
White, E.M.1
Wilson, A.C.2
Greene, S.A.3
McCowan, C.4
Thomas, G.E.5
Cairns, A.Y.6
Ricketts, I.W.7
-
80
-
-
0021015074
-
Prader-Willi Syndrome associated with inversion of chromosome 15
-
Winsor EJZ, Welch JP (1983) Prader-Willi Syndrome associated with inversion of chromosome 15. Clin Genet 24:456-461
-
(1983)
Clin Genet
, vol.24
, pp. 456-461
-
-
Winsor, E.J.Z.1
Welch, J.P.2
-
81
-
-
0026510495
-
Der Einfluß psychotherapeutischer Interventionen auf die Gewichtsreduktion und die Persönlichkeitsentwicklung eines 13jährigen Knaben mit Prader-Willi Syndrome
-
Wurst E, Möslinger D, Widhalm K (1992) Der Einfluß psychotherapeutischer Interventionen auf die Gewichtsreduktion und die Persönlichkeitsentwicklung eines 13jährigen Knaben mit Prader-Willi Syndrome. Clin Pediatr 204:177-180
-
(1992)
Clin Pediatr
, vol.204
, pp. 177-180
-
-
Wurst, E.1
Möslinger, D.2
Widhalm, K.3
-
82
-
-
0029075773
-
Diagnosing Prader-Willi syndrome
-
Young ID (1995) Diagnosing Prader-Willi syndrome. Lancet 345:1590
-
(1995)
Lancet
, vol.345
, pp. 1590
-
-
Young, I.D.1
-
83
-
-
0014284907
-
Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi Syndrome
-
Zellweger H, Schneider HJ (1968) Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi Syndrome. Am J Dis Child 115:588-598
-
(1968)
Am J Dis Child
, vol.115
, pp. 588-598
-
-
Zellweger, H.1
Schneider, H.J.2
-
84
-
-
0022995046
-
The effects of naltrexone, an oral β-endorphin antagonist, in children with the Prader-Willi Syndrome
-
Zlotkin SH, Fettes IM, Stallings VA (1986) The effects of naltrexone, an oral β-endorphin antagonist, in children with the Prader-Willi Syndrome. J Clin Endocrinol Metab 63:1229-1232
-
(1986)
J Clin Endocrinol Metab
, vol.63
, pp. 1229-1232
-
-
Zlotkin, S.H.1
Fettes, I.M.2
Stallings, V.A.3
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