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European Journal of Pediatrics
Volumn 173, Issue 12, 2014, Pages 1565-1568
Primary hypothyroidism: an unusual manifestation of Wolcott–Rallison syndrome
Author keywords

Infantile onset diabetes mellitus; Primary hypothyroidism; Wolcott Rallison Syndrome
Indexed keywords

EID: 84881112907     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-013-2110-8     Document Type: Article
Times cited : (6)
References (10)
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    • Bin-Abbas, B.1    Al-Mulhim, A.2    Al-Ashwal, A.3
  • 3
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    • Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy
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    • Castelnau P, Le Merrer M, Diatloff-Zito C, Marquis E, Tête MJ, Robert JJ (2000) Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy. Eur J Pediatr 159:631–633
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    • Castelnau, P.1    Le Merrer, M.2    Diatloff-Zito, C.3    Marquis, E.4    Tête, M.J.5    Robert, J.J.6
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    • Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature
    • COI: 1:STN:280:DC%2BD2cvnsVWntg%3D%3D, PID: 15384883
    • Iyer S, Korada M, Rainbow L, Kirk J, Brown RM, Shaw N, Barrett TG (2004) Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature. Acta Paediatr 93:1195–1201
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    • COI: 1:CAS:528:DC%2BC3cXptFymt70%3D, PID: 20202148
    • Ozbek MN, Senée V, Aydemir S, Kotan LD, Mungan NO, Yuksel B, Julier C, Topaloglu AK (2010) Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature. Pediatr Diabetes 11:279–285
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    • Ozbek, M.N.1    Senée, V.2    Aydemir, S.3    Kotan, L.D.4    Mungan, N.O.5    Yuksel, B.6    Julier, C.7    Topaloglu, A.K.8
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    • Rubio-Cabezas, O.1    Patch, A.M.2    Minton, J.A.3
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    • Stöss, H.1    Pesch, H.J.2    Pontz, B.3    Otten, A.4    Spranger, J.5
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.