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4. Oculopharyngeal and distal myopathy: a case study from Papua New Guinea. Scrimgeour EM; Mastaglia FL Am J Med Genet; 1984 Apr; 17(4):763-71. PubMed ID: 6720743 [TBL] [Abstract][Full Text] [Related]
5. Spinal muscular atrophy: survival pattern and functional status. Chung BH; Wong VC; Ip P Pediatrics; 2004 Nov; 114(5):e548-53. PubMed ID: 15492357 [TBL] [Abstract][Full Text] [Related]
6. A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy. Echaniz-Laguna A; Rousso E; Anheim M; Cossée M; Tranchant C Neurology; 2005 Apr; 64(8):1458-60. PubMed ID: 15851746 [TBL] [Abstract][Full Text] [Related]
7. A clinical and genetic study of spinal muscular atrophy. Mishra VN; Kalita J; Kesari A; Mitta B; Shankar SK; Misra UK Electromyogr Clin Neurophysiol; 2004; 44(5):307-12. PubMed ID: 15378871 [TBL] [Abstract][Full Text] [Related]
8. The genetic heterogeneity of spinal muscular atrophy (SMA). Zellweger H Birth Defects Orig Artic Ser; 1971 Feb; 7(2):82-9. PubMed ID: 5173130 [TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implications. Rudnik-Schöneborn S; Röhrig D; Morgan G; Wirth B; Zerres K Am J Med Genet; 1994 May; 51(1):70-6. PubMed ID: 8030672 [TBL] [Abstract][Full Text] [Related]
10. [Sex-linked familial form of progressive spinal amyotrophy in adults]. Schanen A; Mikol J; Guiziou C; Vital C; Coquet M; Lagueny A; Julien J; Haguenau M Rev Neurol (Paris); 1984; 140(12):720-7. PubMed ID: 6543025 [TBL] [Abstract][Full Text] [Related]
11. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system. Shaw SW; Cheng PJ; Chang SD; Lin YT; Hung CC; Chen CP; Su YN Acta Obstet Gynecol Scand; 2008; 87(9):960-8. PubMed ID: 18720039 [TBL] [Abstract][Full Text] [Related]
13. A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy. Jansen PH; Joosten EM; Jaspar HH; Vingerhoets HM Ann Neurol; 1986 Oct; 20(4):538-40. PubMed ID: 3789668 [TBL] [Abstract][Full Text] [Related]
14. Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy. Ben Hamida C; Soussi-Yanicostas N; Butler-Browne GS; Bejaoui K; Hentati F; Ben Hamida M Muscle Nerve; 1994 Apr; 17(4):400-10. PubMed ID: 8170486 [TBL] [Abstract][Full Text] [Related]
15. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Wang CH; Carter TA; Das K; Xu J; Ross BM; Penchaszadeh GK; Gilliam TC Ann Neurol; 1997 Jul; 42(1):41-9. PubMed ID: 9225684 [TBL] [Abstract][Full Text] [Related]
16. [Neonatal muscular spinal atrophy: a case report]. Pavone P; Velardita M; Trigilia T; Luca G; Lucenti C; Romeo G; Falsaperla R Pediatr Med Chir; 2004; 26(2):139-41. PubMed ID: 15700740 [TBL] [Abstract][Full Text] [Related]
17. [Chronic spinal amyotrophy with paralysis of the vocal cords: Young-Harper syndrome]. Serratrice G; Pellissier JF; Gastaut JL; Desnuelle C Rev Neurol (Paris); 1984; 140(11):657-8. PubMed ID: 6505493 [TBL] [Abstract][Full Text] [Related]
18. Centronuclear myopathy: follow-up study of a case reported as an early onset myopathy (1966): muscle biopsies in parents and sibs. Mercelis R; Martin JJ; Martin L; Ceuterick C Acta Neurol Belg; 1980; 80(6):348-60. PubMed ID: 7468147 [TBL] [Abstract][Full Text] [Related]
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20. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]. Spiegel R; Hagmann A; Boltshauser E; Moser H Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]