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kw.\*:("Camptodactilia")

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The Tel Hashomer camptodactyly syndrome: report of a new case and review of the literatureBRANCIA PAGNAN, N. A; GOLLOP, T. R; LEDERMAN, H et al.American journal of medical genetics. 1988, Vol 29, Num 2, pp 411-417, issn 0148-7299Article

Beitrag zur Ätiopathologie der Kamptodaktylie. (Fallbeschreibung und Literaturübersicht) = Contribution à l'étiopathologie de la camptodactylie (observation et revue de la littérature) = Etiopathogenesis of camptodactyly (cases and literature review)MARTINI, A. K; NEUSEL, E.Zeitschrift für Orthopädie und ihre Grenzgebiete. 1985, Vol 123, Num 6, pp 943-946, issn 0044-3220Article

Nonoperative treatment of camptodactylyHORI, M; NAKAMURA, R; INOUE, G et al.The Journal of hand surgery (St. Louis, Mo.). 1987, Vol 12, Num 6, pp 1061-1065, issn 0363-5023Article

Camptodactyly in a neurology outpatient clinicLARNER, A. J.International journal of clinical practice (Esher). 2001, Vol 55, Num 9, pp 592-595, issn 1368-5031Article

Muscle weakness and congenital contractures in a case of congenital myastheniaHAGEMAN, G; SMIT, L. M. E; HOOGLAND, R. A et al.Journal of pediatric orthopedics. 1986, Vol 6, Num 2, pp 227-231, issn 0271-6798Article

Camptodactyly, polyepiphyseal dysplasia and mixed crystal deposition diseaseM'HAMED HAMZA; BARDIN, T.Journal of rheumatology. 1989, Vol 16, Num 8, pp 1153-1158, issn 0315-162XArticle

Atteinte axiale avec arthropathie des articulaires postérieures et ankylose osseuse dans un syndrome de camptodactylie, arthropathie, coxa vara et péricardite (CACP)EMAD, Yasser; RAGAB, Yasser; KHALIFA, Maher et al.Revue du rhumatisme (Ed. française). 2013, Vol 80, Num 4, pp 409-412, issn 1169-8330, 4 p.Article

Surgical correction for curly toe using open tenotomy of flexor digitorum brevis tendonTOKIOKA, Kazuyuki; NAKATSUKA, Takashi; TSUJI, Shinsaku et al.Journal of plastic, reconstructive & aesthetic surgery. 2007, Vol 60, Num 12, pp 1317-1322, issn 1748-6815, 6 p.Conference Paper

Neonatal paroxysmal trismus and camptodactyly : The Crisponi syndromeNANNENBERG, Eline A; BIJLMER, Rob; VAN GEEL, Bjorn M et al.American journal of medical genetics. 2005, Vol 133A, Num 1, pp 90-92, issn 0148-7299, 3 p.Article

Recurrence of complex camptopolydactyly in a sibling suggestive of autosomal recessive mode of inheritancePHADKE, Shubha R; AGARWAL, Savita; RATNA DUA PURI et al.American journal of medical genetics. 2003, Vol 116A, Num 1, pp 94-96, issn 0148-7299, 3 p.Article

Camptodactyly, arthropathy, coxa vara, and pericarditis syndrome among egyptiansEL-GARF, Ayman; MAHMOUD, Geilan; GHEITH, Rasha et al.Journal of rheumatology. 2003, Vol 30, Num 5, pp 1081-1086, issn 0315-162X, 6 p.Article

Distal 5q deletion syndrome: Phenotypic correlationsSCHAFER, Irwin A; ROBIN, Nathaniel H; POSCH, James J et al.American journal of medical genetics. 2001, Vol 103, Num 1, pp 63-68, issn 0148-7299Article

The Gordon syndrome revisitedBASEL, Donald; SOBEY, Glenda; GARDNER, Jessica et al.SAMJ. South African medical journal. 2000, Vol 90, Num 9, pp 864-867, issn 0256-9574Article

Camptodactyly : A unifying theory and approach to surgical treatmentSMITH, P. J; GROBBELAAR, A. O.The Journal of hand surgery (St. Louis, Mo.). 1998, Vol 23, Num 1, pp 14-19, issn 0363-5023Article

Schwartz-Jampel syndrome type 2 and stüve-wiedemann syndrome : A case for lumpingSUPERTI-FURGA, A; TENCONI, R; CLEMENTI, M et al.American journal of medical genetics. 1998, Vol 78, Num 2, pp 150-154, issn 0148-7299Article

Les malformations congénitales du membre supérieur. Calendrier de prise en charge = Congenital malformations of upper limb .Timing of managementDE COURTIVRON, B; BONNARD, C; GLORION, B et al.Revue de Médecine de Tours. 1995, Vol 29, Num 9-10, pp 279-282, issn 0557-7721Article

Hereditary camptodactyly masquerading leprosyGURPREET SINGH; VINEET KAUR.Indian Journal of Dermatology Venereology and Leprology. 1993, Vol 59, Num 2, pp 103-104, issn 0378-6323Article

Arthrogryposis, ectodermal dysplasia and other anomalies in two sistersSTOLL, C; ALEMBIK, Y; FINCK, S et al.Genetic counseling. 1992, Vol 3, Num 1, pp 35-39, issn 1015-8146Article

Two siblings with tel hashomer camptodactyly and mitral valve prolapseTORIELLO, H. V; HIFFINGS, J. V; MALVITZ, T et al.American journal of medical genetics. 1990, Vol 36, Num 4, pp 398-403, issn 0148-7299Article

Congenital Hand DifferencesGOLDFARB, Charles A.The Journal of hand surgery (St. Louis, Mo.). 2009, Vol 34A, Num 7, pp 1351-1356, issn 0363-5023, 6 p.Article

Multiple congenital anomalies syndrome : Growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patientsGUION-ALMEIDA, M. L; ZECHI-CEIDE, R. M; RICHIERI-COSTA, A et al.American journal of medical genetics. 1999, Vol 87, Num 1, pp 72-77, issn 0148-7299Article

Airway management in a patient with Hecht's syndromeLANO, C. F; WERKHAVEN, J.Southern medical journal (Birmingham). 1997, Vol 90, Num 12, pp 1241-1243, issn 0038-4348Article

Camptodactyly caused by an anomalous origin of the flexor digitorum superficialis tendon : Case reportHOOGBERGEN, M. M; SCHUURMAN, A. H; KON, M et al.Scandinavian journal of plastic and reconstructive surgery and hand surgery. 1996, Vol 30, Num 1, pp 71-73, issn 0284-4311Article

Novel findings in a patient with weaver or a weaver-like syndromeSCARANO, G; DELLA MONICA, M; LONARDO, F et al.American journal of medical genetics. 1996, Vol 63, Num 2, pp 378-381, issn 0148-7299Article

A syndrome of fibrosing pleuritis, pericarditis, and synovitis with infantile contractures of fingers and toes in 2 sisters : familial fibrosing serositisVERMA, U. N; RAMNATH MISRA; SITARAMAN RADHAKRISNAN et al.Journal of rheumatology. 1995, Vol 22, Num 12, pp 2349-2355, issn 0315-162XArticle

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