268 related articles for article (PubMed ID: 35033190)
1. Managing pregnancy in a spinal muscular atrophy type III patient in Indonesia: a case report.
Setyaningrum CTS; Harahap ISK; Nurputra DK; Rachman IT; Harahap NIF
J Med Case Rep; 2022 Jan; 16(1):14. PubMed ID: 35033190
[TBL] [Abstract][Full Text] [Related]
2. Clinical characterizations of three adults with genetically confirmed spinal muscular atrophy: a case series.
Setyaningrum CTS; Harahap ISK; Nurputra DK; Ar Rochmah M; Sadewa AH; Alkarani GH; Harahap NIF
J Med Case Rep; 2022 Nov; 16(1):435. PubMed ID: 36376972
[TBL] [Abstract][Full Text] [Related]
3. Spinal muscular atrophy in Ghanaian children confirmed by molecular genetic testing: a case series.
Hammond CK; Oppong E; Ameyaw E; Dogbe JA
Pan Afr Med J; 2023; 46():78. PubMed ID: 38282771
[TBL] [Abstract][Full Text] [Related]
4. Monitoring spinal muscular atrophy with three-dimensional optoacoustic imaging.
Nedoschill E; Wagner AL; Danko V; Buehler A; Raming R; Jüngert J; Neurath MF; Waldner MJ; Rother U; Woelfle J; Trollmann R; Knieling F; Regensburger AP
Med; 2024 May; 5(5):469-478.e3. PubMed ID: 38531362
[TBL] [Abstract][Full Text] [Related]
5. Measurement of muscle strength with a handheld dynamometer in patients with chronic spinal muscular atrophy.
Febrer A; Rodriguez N; Alias L; Tizzano E
J Rehabil Med; 2010 Mar; 42(3):228-31. PubMed ID: 20411217
[TBL] [Abstract][Full Text] [Related]
6. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K
J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Spinal muscular atrophy: recent advances and future prospects.
Nicole S; Diaz CC; Frugier T; Melki J
Muscle Nerve; 2002 Jul; 26(1):4-13. PubMed ID: 12115944
[TBL] [Abstract][Full Text] [Related]
9. Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy.
Brahe C; Servidei S; Zappata S; Ricci E; Tonali P; Neri G
Lancet; 1995 Sep; 346(8977):741-2. PubMed ID: 7658877
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. [Spinal muscular atrophy: frequent cause of congenital hypotonia in Morocco].
Sbiti A; Ratbi I; Kriouile Y; Sefiani A
Arch Pediatr; 2011 Dec; 18(12):1261-4. PubMed ID: 22041598
[TBL] [Abstract][Full Text] [Related]
12. Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.
Vill K; Schwartz O; Blaschek A; Gläser D; Nennstiel U; Wirth B; Burggraf S; Röschinger W; Becker M; Czibere L; Durner J; Eggermann K; Olgemöller B; Harms E; Schara U; Kölbel H; Müller-Felber W
Orphanet J Rare Dis; 2021 Mar; 16(1):153. PubMed ID: 33789695
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The predictive value of achieved motor milestones assessed in 441 patients with infantile spinal muscular atrophy types II and III.
Rudnik-Schöneborn S; Hausmanowa-Petrusewicz I; Borkowska J; Zerres K
Eur Neurol; 2001; 45(3):174-81. PubMed ID: 11306862
[TBL] [Abstract][Full Text] [Related]
15. Pregnancy experience in women with spinal muscular atrophy: a case series.
Bencivenga RP; Zoppi D; Russo A; Cassano E; Tozza S; Iodice R; Dubbioso R; Manganelli F; Ruggiero L
Acta Myol; 2023; 42(2-3):60-64. PubMed ID: 38090543
[TBL] [Abstract][Full Text] [Related]
16. [Infantile spinal muscular atrophy].
Barois A; Estournet B; Duval-Beaupère G; Bataille J; Leclair-Richard D
Rev Neurol (Paris); 1989; 145(4):299-304. PubMed ID: 2660222
[TBL] [Abstract][Full Text] [Related]
17. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy.
Omran H; Ketelsen UP; Heinen F; Sauer M; Rudnik-Schöneborn S; Wirth B; Zerres K; Kratzer W; Korinthenberg R
J Child Neurol; 1998 Jul; 13(7):327-31. PubMed ID: 9701481
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Prenatal diagnosis for risk of spinal muscular atrophy.
Cuscó I; Barceló MJ; Soler C; Parra J; Baiget M; Tizzano E
BJOG; 2002 Nov; 109(11):1244-9. PubMed ID: 12452462
[TBL] [Abstract][Full Text] [Related]
20. Onasemnogene abeparvovec-xioi: a gene replacement strategy for the treatment of infants diagnosed with spinal muscular atrophy.
Schwartz M; Likhite S; Meyer K
Drugs Today (Barc); 2021 Jun; 57(6):387-399. PubMed ID: 34151905
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]