SCOPUS 정보 검색 플랫폼

Volumn 7, Issue 3, 1998, Pages 209-211

A case of multiple intestinal atresias, brain anomalies, mental retardation, growth hormone deficiency and clitoris hypertrophy

(5) Guala, A a Licardi, G a Maghnie, M b Minniti, S b Danesino, C c

a Ospedale Civile (Italy)

b FONDAZIONE IRCCS POLICLINICO SAN MATTEO (Italy)

c Biologia Generale e Genetica Medica (Italy)

Author keywords

Brain anomalies; GH deficiency; Multiple intestinal atresias

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CHILD; CLITORIS; FEMALE; GROWTH HORMONE DEFICIENCY; HUMAN; INTESTINE ATRESIA; JEJUNOILEOSTOMY; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; BRAIN; CHILD; CHILD, PRESCHOOL; CLITORIS; FEMALE; GROWTH HORMONE; HUMANS; HYPERTROPHY; INFANT, NEWBORN; INTESTINAL ATRESIA; MENTAL RETARDATION;

EID: 0031816784 PISSN: 09628827 EISSN: None Source Type: Journal
DOI: 10.1097/00019605-199807000-00010 Document Type: Article

Times cited : (1)

References (7)

1
- 15644381248
- Multiple intestinal atresias
- Buyse MM editor. Dover MA: Blackwell Scientific Publications
- Der Kaloustian VM, Mishalany HG (1990). Multiple intestinal atresias. In: Buyse MM editor. Birth defect encyclopedia Dover MA: Blackwell Scientific Publications, p. 976.
- (1990) Birth defect Encyclopedia , pp. 976
- Der Kaloustian, V.M.¹ Mishalany, H.G.²

2
- 0029007429
- Familial intestinal polyatresia syndrome
- Güngör N, Balci S, Tanyel FC, Gögüs S (1995). Familial intestinal polyatresia syndrome. Clin Genet 47:245-247.
- (1995) Clin Genet , vol.47 , pp. 245-247
- Güngör, N.¹ Balci, S.² Tanyel, F.C.³ Gögüs, S.⁴

3
- 0025321334
- Craniosynostosis, agenesis of the corpus callosum, severe mental retardation, distinctive facies, camptodactyly, and hypogonadism
- Lin AE, Gettig E (1990). Craniosynostosis, agenesis of the corpus callosum, severe mental retardation, distinctive facies, camptodactyly, and hypogonadism. Am J Med Genet 35:582-585.
- (1990) Am J Med Genet , vol.35 , pp. 582-585
- Lin, A.E.¹ Gettig, E.²

4
- 0025181206
- Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: Study of a family
- Moreno LA, Gottrand F, Turck D, Manouvrier-Hanu S, Mazingue F, Morisot C, Le Deist F, Ricour C, Nihoul-Feketé C, Debeugny P, Griscelli C, Farriaux JP (1990). Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family. Am J Med Genet 37:143-146.
- (1990) Am J Med Genet , vol.37 , pp. 143-146
- Moreno, L.A.¹ Gottrand, F.² Turck, D.³ Manouvrier-Hanu, S.⁴ Mazingue, F.⁵ Morisot, C.⁶ Le Deist, F.⁷ Ricour, C.⁸ Nihoul-Feketé, C.⁹ Debeugny, P.¹⁰ Griscelli, C.¹¹ Farriaux, J.P.¹²

5
- 0023200826
- Familial apple peel jejunal atresia: Surgical, genetic, and radiographie aspects
- Seashore JH, Collins FS, Markowitz RI, Seashore MR (1987). Familial apple peel jejunal atresia: surgical, genetic, and radiographie aspects. Pediatrics 80:540-544.
- (1987) Pediatrics , vol.80 , pp. 540-544
- Seashore, J.H.¹ Collins, F.S.² Markowitz, R.I.³ Seashore, M.R.⁴

6
- 0030443298
- Further evidence for a syndrome of 'apple peel' intestinal atresia, ocular anomalies and microcephaly
- Slee J, Goldblatt J (1996). Further evidence for a syndrome of 'apple peel' intestinal atresia, ocular anomalies and microcephaly. Clin Genet 50:260-262.
- (1996) Clin Genet , vol.50 , pp. 260-262
- Slee, J.¹ Goldblatt, J.²

7
- 0027496345
- Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly
- Stromme P, Dahl E, Flage T, Stene-Johansen H (1993). Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly. Clin Genet 44:208-210.
- (1993) Clin Genet , vol.44 , pp. 208-210
- Stromme, P.¹ Dahl, E.² Flage, T.³ Stene-Johansen, H.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.