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.
5. [The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis]. Blennow ES; Bui TH; Söderhäll S; Anvret M; Nordenskjöld M Lakartidningen; 1993 Jan; 90(4):269-75. PubMed ID: 8433608 [No Abstract] [Full Text] [Related]
6. [Early myoclonic encephalopathy and spinal muscular atrophy type I]. Bado M; Bruno C; Morreale G; Parisi F; Minetti C; Cordone G Minerva Pediatr; 1995 Jun; 47(6):233-8. PubMed ID: 7476749 [TBL] [Abstract][Full Text] [Related]
7. [Diagnostic progress in spinal muscular atrophy]. Gergont A; Kaciński M; Steczkowska-Klucznik M Przegl Lek; 2001; 58(11):989-91. PubMed ID: 11987841 [TBL] [Abstract][Full Text] [Related]
8. [A molecular genetic analysis of spinal muscular atrophy (SMA) in families at high risk from different regions of Ukraine]. Ekshiian AIu; Livshits LA; Bychkova AM; Afanas'eva NA; Bariliak IR Tsitol Genet; 1997; 31(6):75-81. PubMed ID: 9591348 [TBL] [Abstract][Full Text] [Related]
9. Progressive subcutaneous and periarticular calcifications in a patient with spinal muscular atrophy type III. Boltshauser E; Gehrmann J; Steinlin M; Eich G; Spiegel R Neuropediatrics; 1995 Dec; 26(6):331-2. PubMed ID: 8719752 [No Abstract] [Full Text] [Related]
10. Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia. Sertić J; Barisić N; Sostarko M; Bosnjak N; Culić V; Cvitanović L; Ferencak G; Brzović Z; Stavljenić-Rukavina A Coll Antropol; 1997 Dec; 21(2):487-92. PubMed ID: 9439064 [TBL] [Abstract][Full Text] [Related]
11. Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene. Yiu EM; Ravat S; Ryan MM; Shield LK; Smith LJ; Kornberg AJ Muscle Nerve; 2008 Jul; 38(1):930-2. PubMed ID: 18508340 [TBL] [Abstract][Full Text] [Related]
12. Clinical and genetic study of spinal muscular atrophies in Oman. Koul R; Al Futaisi A; Chacko A; Rao V; Simsek M; Muralitharan S; Ganguly SS; Bayoumi R J Child Neurol; 2007 Oct; 22(10):1227-30. PubMed ID: 17940251 [TBL] [Abstract][Full Text] [Related]
13. [Gene diagnosis for spinal muscular atrophy and its application study]. Cao DH; Ren MH; Lin CK; Cui WT; Ma HW; Wu YY; Jin CL Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):306-9. PubMed ID: 19504445 [TBL] [Abstract][Full Text] [Related]
14. [Study of NAIP gene in spinal muscular atrophy]. Ma H; Wang Y; Mi Z; Wu Y; Zhao P; Zhao S; Jiang M; Li Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Apr; 16(2):97-8. PubMed ID: 10194256 [TBL] [Abstract][Full Text] [Related]
15. [Perspectives in medical genetics: the new genetics]. Bueno M; Pérez-González JM Rev Med Univ Navarra; 1992; 37(4):181-9. PubMed ID: 1298036 [No Abstract] [Full Text] [Related]
16. A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3). Jedrzejowska M; Ryniewicz B; Kabzińska D; Drac H; Hausmanowa-Petrusewicz I; Kochański A Neuromuscul Disord; 2008 Apr; 18(4):339-41. PubMed ID: 18337101 [TBL] [Abstract][Full Text] [Related]