These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. 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]
3. [Clinical study of 83 cases with spinal muscular atrophy in children]. Li H; Wang HL; Shan CM Zhonghua Er Ke Za Zhi; 2004 Oct; 42(10):762-4. PubMed ID: 16221347 [TBL] [Abstract][Full Text] [Related]
5. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Gilliam TC; Brzustowicz LM; Castilla LH; Lehner T; Penchaszadeh GK; Daniels RJ; Byth BC; Knowles J; Hislop JE; Shapira Y Nature; 1990 Jun; 345(6278):823-5. PubMed ID: 1972783 [TBL] [Abstract][Full Text] [Related]
6. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals. Hahnen E; Forkert R; Marke C; Rudnik-Schöneborn S; Schönling J; Zerres K; Wirth B Hum Mol Genet; 1995 Oct; 4(10):1927-33. PubMed ID: 8595417 [TBL] [Abstract][Full Text] [Related]
7. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings. Rudnik-Schöneborn S; Forkert R; Hahnen E; Wirth B; Zerres K Neuropediatrics; 1996 Feb; 27(1):8-15. PubMed ID: 8677029 [TBL] [Abstract][Full Text] [Related]
8. Apparent SMA I unlinked to 5q. Cobben JM; Scheffer H; de Visser M; Begeer JH; Molenaar WM; van der Steege G; Buys CH; van Ommen GJ; Ten Kate LP J Med Genet; 1994 Mar; 31(3):242-4. PubMed ID: 8014975 [TBL] [Abstract][Full Text] [Related]
14. Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion. García-Cabezas MA; García-Alix A; Martín Y; Gutiérrez M; Hernández C; Rodríguez JI; Morales C Acta Neuropathol; 2004 May; 107(5):475-8. PubMed ID: 14968368 [TBL] [Abstract][Full Text] [Related]
15. Prenatal prediction of spinal muscular atrophy. Daniels RJ; Suthers GK; Morrison KE; Thomas NH; Francis MJ; Mathew CG; Loughlin S; Heiberg A; Wood D; Dubowitz V J Med Genet; 1992 Mar; 29(3):165-70. PubMed ID: 1348091 [TBL] [Abstract][Full Text] [Related]
16. Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophy. Paul DA; Goldsmith LS; Miles DK; Moser AB; Spiro AJ; Grover WD Pediatr Neurol; 1993; 9(6):496-7. PubMed ID: 7605563 [TBL] [Abstract][Full Text] [Related]
17. [Contribution of the electromyogram in the diagnosis of infantile spinal muscular atrophy in the neonatal period]. Renault F; Chartier JP; Harpey JP Arch Pediatr; 1996 Apr; 3(4):319-23. PubMed ID: 8762951 [TBL] [Abstract][Full Text] [Related]
18. Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration. Rudnik-Schöneborn S; Wirth B; Röhrig D; Saule H; Zerres K Neuromuscul Disord; 1995 Jan; 5(1):19-23. PubMed ID: 7719136 [TBL] [Abstract][Full Text] [Related]
19. The motor neuron response to SMN1 deficiency in spinal muscular atrophy. Kang PB; Gooch CL; McDermott MP; Darras BT; Finkel RS; Yang ML; Sproule DM; Chung WK; Kaufmann P; de Vivo DC; Muscle Nerve; 2014 May; 49(5):636-44. PubMed ID: 23893312 [TBL] [Abstract][Full Text] [Related]
20. Type I spinal muscular atrophy can mimic sensory-motor axonal neuropathy. Anagnostou E; Miller SP; Guiot MC; Karpati G; Simard L; Dilenge ME; Shevell MI J Child Neurol; 2005 Feb; 20(2):147-50. PubMed ID: 15794183 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]