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24. Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1. Brown KA; al-Gazali LI; Moynihan LM; Lench NJ; Markham AF; Mueller RF J Med Genet; 1997 Aug; 34(8):685-7. PubMed ID: 9279765 [TBL] [Abstract][Full Text] [Related]
26. Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2. Sigaudy S; Moncla A; Fredouille C; Bourlière B; Lambert JC; Philip N Clin Dysmorphol; 1998 Oct; 7(4):257-62. PubMed ID: 9823491 [TBL] [Abstract][Full Text] [Related]
27. Schwartz-Jampel syndrome: an atypical form? Figuera LE; Jimenez-Gil FJ; García-Cruz MO; Cantú JM Am J Med Genet; 1993 Sep; 47(4):526-8. PubMed ID: 8256816 [TBL] [Abstract][Full Text] [Related]
28. Spectrum of Schwartz-Jampel syndrome includes micromelic chondrodysplasia, kyphomelic dysplasia, and Burton disease. Spranger J; Hall BD; Häne B; Srivastava A; Stevenson RE Am J Med Genet; 2000 Oct; 94(4):287-95. PubMed ID: 11038441 [TBL] [Abstract][Full Text] [Related]
29. [Schwartz-Jampel syndrome. Positive therapeutic effect of diacarb]. Aver'ianov IuN Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(10):1498-1502. PubMed ID: 716726 [TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis of Schwartz-Jampel syndrome with early manifestation. Hunziker UA; Savoldelli G; Boltshauser E; Giedion A; Schinzel A Prenat Diagn; 1989 Feb; 9(2):127-31. PubMed ID: 2646626 [TBL] [Abstract][Full Text] [Related]
33. Schwartz-Jampel syndrome. Bastola P Kathmandu Univ Med J (KUMJ); 2010; 8(31):348-51. PubMed ID: 22610743 [TBL] [Abstract][Full Text] [Related]
34. The effect of the Schwartz-Jampel syndrome on masticatory and facial musculatures--an electromyographic analysis. Regalo SC; Vitti M; Semprini M; de Mattos Mda G; Hallak JE; Brandão C; Serrano KV Electromyogr Clin Neurophysiol; 2005; 45(3):183-9. PubMed ID: 15981691 [TBL] [Abstract][Full Text] [Related]
35. Resistance to rocuronium in a child with Schwartz-Jampel syndrome type 1 B. Eikermann M; Bredendiek M; Schaper J; Hövel M; Peters J Neuropediatrics; 2002 Feb; 33(1):43-6. PubMed ID: 11930277 [TBL] [Abstract][Full Text] [Related]
36. Schwartz-Jampel syndrome: report of five cases. Reed UC; Reimao R; Espindola AA; Kok F; Ferreira LG; Resende MB; Messias TC; Carvalho MS; Diament A; Scaff M; Marie SK Arq Neuropsiquiatr; 2002 Sep; 60(3-B):734-8. PubMed ID: 12364940 [TBL] [Abstract][Full Text] [Related]
37. Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case report. Ho NC; Sandusky S; Madike V; Francomano CA; Dalakas MC BMC Neurol; 2003 Jul; 3():3. PubMed ID: 12839625 [TBL] [Abstract][Full Text] [Related]
38. Schwartz-Jampel syndrome: report of one case. Yang MT; Yang CC; Chu LW; Lee WT; Young C; Wang PJ Acta Paediatr Taiwan; 2002; 43(4):220-3. PubMed ID: 12238912 [TBL] [Abstract][Full Text] [Related]