Multiple Pterygium syndrome: an overviewRAMER, J. C; LADDA, R. L; DEMUTH, W. W et al.American journal of diseases of children (1960). 1988, Vol 142, Num 7, pp 794-798, issn 0002-922XArticle

Syndrome de casse-noisette = Nutcracker syndromeBERNARD, Clémence; DE SAINT ROMAN, Charlotte; GERVAISE, Alban et al.La Presse médicale (1983). 2013, Vol 42, Num 4, pp 487-488, issn 0755-4982, 2 p., CAH1Article

Un syndrome caveREZGUI-MARHOUL, Lamia; DOUIRA, Wiém; BOUSLAMA, Kamel et al.Concours médical (Paris). 2004, Vol 126, Num 2, pp 99-101, issn 0010-5309, 3 p.Article

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2BALLIF, Blake C; HORNOR, Sara A; GRAHAM, John M et al.Nature genetics. 2007, Vol 39, Num 9, pp 1071-1073, issn 1061-4036, 3 p.Article

Leriche SyndromeFREDERICK, Michael; NEWMAN, John; KOHLWES, Jeffrey et al.Journal of general internal medicine. 2010, Vol 25, Num 10, pp 1102-1104, issn 0884-8734, 3 p.Article

Kounis SyndromeLOPEZ, Pablo R; PEIRIS, Alan N.Southern medical journal (Birmingham, Ala. Print). 2010, Vol 103, Num 11, pp 1148-1155, issn 0038-4348, 8 p.Article

Molecular bases of progeroid syndromesNAVARRO, Claire L; CAU, Pierre; LEVYL, Nicolas et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R151-R161, NS2Article

Clinical and molecular genetic features of ARC syndromeGISSEN, Paul; TEE, Louise; FITZPATRICK, David et al.Human genetics. 2006, Vol 120, Num 3, pp 396-409, issn 0340-6717, 14 p.Article

CARD15 mutations in Blau syndromeMICELI-RICHARD, Corinne; LESAGE, Suzanne; RYBOJAD, Michel et al.Nature genetics. 2001, Vol 29, Num 1, pp 19-20, issn 1061-4036Article

Syndrome de Wellens = Wellens syndromePEYRONY, O; ELEZI, A; TABOULET, P et al.Annales françaises de médecine d'urgence. 2013, Vol 3, Num 5, issn 2108-6524, p. 321Article

DCTN1 mutations in Perry syndromeFARRER, Matthew J; HULIHAN, Mary M; TSUBOI, Yoshio et al.Nature genetics. 2009, Vol 41, Num 2, pp 163-165, issn 1061-4036, 3 p.Article

Syndrome post-poliomyélite : Handicap = Postpolio syndrome F Genêt, L. Théfenne, F Boyer : HandicapGENET, François; THEFENNE, Laurent; BOYER, François et al.La Revue du praticien (Paris). 2009, Vol 59, Num 8, pp 1085-1086, issn 0035-2640, 2 p.Article

Shapiro syndromeSAYRE SHENOY, Chetan.QJM (Oxford. 1994. Print). 2008, Vol 101, Num 1, pp 61-62, issn 1460-2725, 2 p.Article

Rumination Syndrome : An Emerging Case ScenarioATTRI, Navneet; RAVIPATI, M; AGRAWAL, Preeti et al.Southern medical journal (Birmingham). 2008, Vol 101, Num 4, pp 432-435, issn 0038-4348, 4 p.Article

Neuroleptic malignant syndromeSTRAWN, Jeffrey R; KECK, Paul E; CAROFF, Stanley N et al.The American journal of psychiatry. 2007, Vol 164, Num 6, pp 870-876, issn 0002-953X, 7 p.Article

Ganser's syndromeDWYER, Justin; REID, Steven.Lancet (British edition). 2004, Vol 364, Num 9432, pp 471-473, issn 0140-6736, 3 p.Article

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndromeARBOLEDA, Valerie A; LEE, Hane; DELL'ANGELICA, Esteban C et al.Nature genetics. 2012, Vol 44, Num 7, pp 788-792, issn 1061-4036, 5 p.Article

Nutcracker Phenomenon and Nutcracker SyndromeKURKLINSKY, Andrew K; ROOKE, Thom W.Mayo Clinic proceedings. 2010, Vol 85, Num 6, pp 552-559, issn 0025-6196, 8 p.Article

Síndrome de Cobb o angiomatosis cutáneo-meningo-espinal = Cobb syndrome or cutaneomeningospinal angiomatosisPALANCA ARIAS, D; RIUS GORDILLO, N; GARCIA FRUCTUOSO, G et al.Anales de pediatria (2003. Ed. impresa). 2010, Vol 73, Num 2, pp 109-111, issn 1695-4033, 3 p.Article

An Unusual Presentation of Trisomy 13COLLINSWORTH, Amy; LACASSIE, Yves.American journal of medical genetics. Part A. 2008, Vol 146, Num 11, pp 1490-1492, issn 1552-4825, 3 p.Article

The syndrome of inappropriate antidiuresisELLISON, David H; BERL, Tomas.The New England journal of medicine. 2007, Vol 356, Num 20, pp 2064-2072, issn 0028-4793, 9 p.Article

Le syndrome post-chute : comment le reconnaître et le traiter : Gérontologie = Post-fall syndrome : how to recognize and treat it?MORISOD, J; COUTAZ, M.Revue médicale suisse. 2007, Vol 3, Num 132, issn 1660-9379, 2531-2536 [4 p.]Article

A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosisCLAYTON-SMITH, J; DONNAI, D.Journal of medical genetics. 1989, Vol 26, Num 5, pp 339-342, issn 0022-2593, 4 p.Article

GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible new recessively inherited MCA/MR syndromeVERLOES, A; DELFORTRIE, J; LAMBOTTE, C et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 15-18, issn 0148-7299, 4 p.Article

Le syndrome de 2^ème portée au 1^er plan des préoccupationsBOULOT, Sylviane.Tech porc. 2011, Num 1, pp 22-23, issn 2119-8772, 2 p.Article