Corticotroph deficiencyLEFEBVRE, Hervé.Annales d'endocrinologie. 2012, Vol 73, Num 2, pp 135-137, issn 0003-4266, 3 p.Conference Paper

Diagnostic and therapeutic challenges of acquired thyrotropic deficiencyPERSANI, Luca; BONOMI, Marco; RADIN, Raffaella et al.Annales d'endocrinologie. 2012, Vol 73, Num 2, pp 138-140, issn 0003-4266, 3 p.Conference Paper

Treatment of corticotroph deficiencyOULEGHZAL, Hassan; ROSALES, Caroline; RAFFIN-SANSON, Marie-Laure et al.Annales d'endocrinologie. 2012, Vol 73, Num 1, pp 12-19, issn 0003-4266, 8 p.Article

Acromionectomy and Deltoid Deficiency : A SolutionFORSYTHE, Brian; LAVERY, Kyle P; WARNER, Jon J. P et al.Clinical orthopaedics and related research. 2009, Vol 467, Num 5, pp 1334-1340, issn 0009-921X, 7 p.Article

Brca2 (XRCC11) deficiency results in enhanced mutagenesisKRAAKMAN-VAN DER ZWET, Maria; WIEGANT, Wouter W; ZDZIENICKA, Małgorzata Z et al.Mutagenesis. 2003, Vol 18, Num 6, pp 521-525, issn 0267-8357, 5 p.Article

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Factor XI Deficiency and Obstetrical AnesthesiaSINGH, Amarjeet; HARNETT, Miriam J; CONNORS, Jean M et al.Anesthesia and analgesia. 2009, Vol 108, Num 6, pp 1882-1885, issn 0003-2999, 4 p.Article

Acylcarnitine deficiency in chronic fatigue syndromeKURATSUNE, H; YAMAGUTI, K; TAKAHASHI, M et al.Clinical infectious diseases. 1994, Vol 18, pp S62-S67, issn 1058-4838, SUP1Conference Paper

Delirious deficiencyQUESENBERRY OLSEN, Robin; REGIS, Joanna T.Lancet (British edition). 2010, Vol 376, Num 9749, issn 0140-6736, p. 1362Article

Nonclassical 21-hydroxylase deficiencyNEW, Maria I.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 11, pp 4205-4214, issn 0021-972X, 10 p.Article

Mycobacterial Disease and Impaired IFN-γ Immunity in Humans with Inherited ISG15 DeficiencyBOGUNOVIC, Dusan; BYUN, Minji; MANSOURI, Nahal et al.Science (Washington, D.C.). 2012, Vol 337, Num 6102, pp 1684-1688, issn 0036-8075, 5 p.Article

Commission des comptes de la Sécurité sociale du 28 septembre 2005ARRCO - EXTRAITS DE DOCUMENTATION. 2005, Num 17, pp 17-30, issn 1155-1887, 14 p.Article

Primary mucociliary transport failureUMEKI, S.Respiration (Basel). 1988, Vol 54, Num 4, pp 220-225, issn 0025-7931Article

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HNF1B Deficiency Causes Ciliary Defects in Human CholangiocytesROELANDT, Philip; ANTONIOU, Aline; PONTOGLIO, Marco et al.Hepatology (Baltimore, Md.). 2012, Vol 56, Num 3, pp 1178-1181, issn 0270-9139, 4 p.Article

Congenital Monocular Elevation DeficiencyJAE HYOUNG KIM; HWANG, Jeong-Min.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 3, pp 580-584, issn 0161-6420, 5 p.Article

Iodine-deficiency disordersZIMMERMANN, Michael B; JOOSTE, Pieter L; PANDAV, Chandrakant S et al.Lancet (British edition). 2008, Vol 372, Num 9645, pp 1251-1262, issn 0140-6736, 12 p.Article

Lipin deficiency impairs diurnal metabolic fuel switchingJUN XU; LEE, W. N. Paul; PHAN, Jack et al.Diabetes (New York, NY). 2006, Vol 55, Num 12, pp 3429-3438, issn 0012-1797, 10 p.Article

Pbx3 deficiency results in central hypoventilationJOON WHAN RHEE; ARATA, Akiko; SELLERI, Licia et al.The American journal of pathology. 2004, Vol 165, Num 4, pp 1343-1350, issn 0002-9440, 8 p.Article

Déficit familial en facteur XIIIZAFAD, Saadia; MADANI, Abdellah; HARIF, Mohamed et al.MTP. Médecine thérapeutique pédiatrie. 2001, Vol 4, Num 5, pp 374-376, issn 1286-5494Article

Mangelsituation: vitamin B₁NEESER, G; ECKART, J; LICHTWARCK-ASCHOFF, M et al.Contributions to infusion therapy. 1989, Vol 25, pp 142-160, 19 p.Article

Haploinsufficiency of C0Q4 causes coenzyme Q10 deficiencySALVIATI, Leonardo; TREVISSON, Eva; SACCONI, Sabrina et al.Journal of medical genetics. 2012, Vol 49, Num 3, pp 187-191, issn 0022-2593, 5 p.Article

Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiencyMEIMARIDOU, Eirini; KOWALCZYK, Julia; CHAPPLE, J. Paul et al.Nature genetics. 2012, Vol 44, Num 7, pp 740-742, issn 1061-4036, 3 p.Article

Montreal pllatelet syndrome: a defect in calcium-activated neutral proteinase (calpain)RICE OKITA, J; FROJMOVIC, M. M; KRISTOPEIT, S et al.Blood. 1989, Vol 74, Num 2, pp 715-721, issn 0006-4971Article

Copper deficiencyCHHETRI, S. K; MILLS, R. J; SHAUNAK, S et al.BMJ (Overseas and retired doctors ed.). 2014, Vol 348, Num 7963, pp 37-39, issn 1759-2151, 3 p.Article