SCOPUS 정보 검색 플랫폼

American Journal of Diseases of Children

Volumn 131, Issue 7, 1977, Pages 798-800

Prader-Willi Syndrome: Variable Severity and Recurrence Risk

(2) Clarren, Sterling K a Smith, David W a

a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSIS; FOREHEAD; FRONTAL CORTEX; GENETIC COUNSELING; HYPOGONADISM; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; MICROPENIS; MUSCLE HYPOTONIA; PRADER WILLI SYNDROME; PREVENTION; RECURRENCE RISK; SCALP HAIR; SIBLING;

ADOLESCENT; ADULT; CASE REPORT; CHILD; CHILD, PRESCHOOL; FEMALE; HUMAN; MALE; PRADER-WILLI SYNDROME; RISK; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0017646315 PISSN: 00968994 EISSN: 23742976 Source Type: Journal
DOI: 10.1001/archpedi.1977.02120200080018 Document Type: Article

Times cited : (32)

References (20)

1
- 0015387610
- Prader-Willi syndrome
- Hall BD, Smith DW: Prader-Willi syndrome. J Pediatr 81:286-293, 1972.
- (1972) J Pediatr , vol.81 , pp. 286-293
- Hall, B.D.¹ Smith, D.W.²

2
- 0003178097
- Factors associated with early and late fetal loss
- Shapiro S, Levine H, Abramowicz M: Factors associated with early and late fetal loss. Adv Planned Parenthood 4:45-64, 1970.
- (1970) Adv Planned Parenthood , vol.4 , pp. 45-64
- Shapiro, S.¹ Levine, H.² Abramowicz, M.³

3
- 0015881282
- Scalp hair patterning as a clue to early fetal brain development
- Smith DW, Gong BT: Scalp hair patterning as a clue to early fetal brain development. J Pediatr 83:375-378, 1973.
- (1973) J Pediatr , vol.83 , pp. 375-378
- Smith, D.W.¹ Gong, B.T.²

4
- 0000927260
- Ein syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter
- Prader A, Labhart A, Willi H: Ein syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz Med Wochenschr 86:1260-1261, 1956.
- (1956) Schweiz Med Wochenschr , vol.86 , pp. 1260-1261
- Prader, A.¹ Labhart, A.² Willi, H.³

5
- 84913772014
- Metabolic and genetic syndromes of overgrowth
- in Gardner LI (ed): Philadelphia, WB Saunders Co
- Ichiba Y, Gardner LI: Metabolic and genetic syndromes of overgrowth, in Gardner LI (ed): Endocrine and Genetic Diseases of Childhood and Adolescence. Philadelphia, WB Saunders Co, 1975, p 1325.
- (1975) Endocrine and Genetic Diseases of Childhood and Adolescence , pp. 1325
- Ichiba, Y.¹ Gardner, L.I.²

6
- 0242367773
- Philadelphia, WB Saunders Co
- Smith DW: Recognizable Patterns of Human Malformation. Philadelphia, WB Saunders Co, 1970, p 88.
- (1970) Recognizable Patterns of Human Malformation , pp. 88
- Smith, D.W.¹

7
- 0014284907
- Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome
- Zellweger H, Schneider HJ: Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome. Am J Dis Child 115:588-598, 1968.
- (1968) Am J Dis Child , vol.115 , pp. 588-598
- Zellweger, H.¹ Schneider, H.J.²

8
- 0015875511
- Prader-Willi syndrome in infant monozygotic twins
- Brissenden JE, Levy EP: Prader-Willi syndrome in infant monozygotic twins. Am J Dis Child 126:110-112, 1973.
- (1973) Am J Dis Child , vol.126 , pp. 110-112
- Brissenden, J.E.¹ Levy, E.P.²

9
- 84946964010
- Prader-Willi syndrome
- Gorlin R, Sedano H, Boggs W: Prader-Willi syndrome. Pediatric Ann 4:219, 1975.
- (1975) Pediatric Ann , vol.4 , pp. 219
- Gorlin, R.¹ Sedano, H.² Boggs, W.³

10
- 0015031551
- Prader-Willi syndrome
- Jancar J: Prader-Willi syndrome. J Ment Defic Res 15:20-27, 1971.
- (1971) J Ment Defic Res , vol.15 , pp. 20-27
- Jancar, J.¹

11
- 0014246316
- Le syndrome de Prader Labhart et Willi (studie de onze observations)
- Gabilan JC, Royer P: Le syndrome de Prader Labhart et Willi (studie de onze observations). Arch Fr Pediatr 25:121-149, 1968.
- (1968) Arch Fr Pediatr , vol.25 , pp. 121-149
- Gabilan, J.C.¹ Royer, P.²

12
- 75549111530
- Le diabete sucre dans le syndrome de Willi-Prader
- Royer P: Le diabete sucre dans le syndrome de Willi-Prader. Journ Annu Diabetol Hotel Dieu. 4:91-99, 1963.
- (1963) Journ Annu Diabetol Hotel Dieu , vol.4 , pp. 91-99
- Royer, P.¹

13
- 0014323796
- Prader-Willi syndrome
- Landwirth J, Schwartz AH, Grunt JA: Prader-Willi syndrome. Am J Dis Child 116:211-217, 1968.
- (1968) Am J Dis Child , vol.116 , pp. 211-217
- Landwirth, J.¹ Schwartz, A.H.² Grunt, J.A.³

14
- 76549151230
- Hypogenital dystrophy with diabetic tendency
- Evans PR: Hypogenital dystrophy with diabetic tendency. Guys Hosp Rep 113:207-222, 1964.
- (1964) Guys Hosp Rep , vol.113 , pp. 207-222
- Evans, P.R.¹

15
- 0016189910
- Prader-Willi-Labhart-syndrome im. Sauglingsalter
- Haberfellner H, Glatzl J, Unterkircher R: Prader-Willi-Labhart-syndrome im. Sauglingsalter. Paediatr Paedol 9:123-129, 1974.
- (1974) Paediatr Paedol , vol.9 , pp. 123-129
- Haberfellner, H.¹ Glatzl, J.² Unterkircher, R.³

16
- 84937665168
- Prader-Willi syndrome
- Murdoch JL: Prader-Willi syndrome. Birth Defects 5:213, 1969.
- (1969) Birth Defects , vol.5 , pp. 213
- Murdoch, J.L.¹

17
- 0014060957
- Prader-Willi syndrome
- Hoefnagel D, Costello PJ, Hatoum K: Prader-Willi syndrome. J Ment Defic Res 11:1-11, 1967.
- (1967) J Ment Defic Res , vol.11 , pp. 1-11
- Hoefnagel, D.¹ Costello, P.J.² Hatoum, K.³

18
- 73049128499
- Benign congenital hypotonia with chromosomal anomaly
- Dunn HG, Denys KF, Auersperg N, et al: Benign congenital hypotonia with chromosomal anomaly. Pediatrics 28:578-591, 1961.
- (1961) Pediatrics , vol.28 , pp. 578-591
- Dunn, H.G.¹ Denys, K.F.² Auersperg, N.³

19
- 4344575593
- Prader-Willi syndrome in boy of ten with prediabetes
- Forssman H, Hagberg B: Prader-Willi syndrome in boy of ten with prediabetes. Acta Paediatr 58:70-78, 1964.
- (1964) Acta Paediatr , vol.58 , pp. 70-78
- Forssman, H.¹ Hagberg, B.²

20
- 4644306776
- Hypotonia, obesity, hypogonadism and mental retardation in childhood
- Laurance BM: Hypotonia, obesity, hypogonadism and mental retardation in childhood. Arch Dis Child 36:690, 1961.
- (1961) Arch Dis Child , vol.36 , pp. 690
- Laurance, B.M.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.