BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

308 related articles for article (PubMed ID: 17761658)

  • 1. Spinal muscular atrophy genetic counseling access and genetic knowledge: parents' perspectives.
    Meldrum C; Scott C; Swoboda KJ
    J Child Neurol; 2007 Aug; 22(8):1019-26. PubMed ID: 17761658
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Prenatal diagnosis of spinal muscular atrophy (SMA) -- indications, restrictions, interpretation of results].
    Jedrzejowska M; Zimowski J; Wiszniewski W; Sielska D; Bal J; Mazurczak T; Hausmanowa-Petrusewicz I; Zaremba J
    Med Wieku Rozwoj; 2004; 8(3 Pt 2):651-61. PubMed ID: 15858238
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Raising obstetricians' awareness of spinal muscular atrophy: towards early detection and reproductive planning.
    Parra J; Tizzano EF
    J Matern Fetal Neonatal Med; 2012 Dec; 25(12):2555-8. PubMed ID: 22712688
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study.
    Qian Y; McGraw S; Henne J; Jarecki J; Hobby K; Yeh WS
    BMC Neurol; 2015 Oct; 15():217. PubMed ID: 26499462
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Parents' advice to healthcare professionals working with children who have spinal muscular atrophy.
    Hjorth E; Kreicbergs U; Sejersen T; Lövgren M
    Eur J Paediatr Neurol; 2018 Jan; 22(1):128-134. PubMed ID: 29146237
    [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. Clinical and molecular diagnosis of spinal muscular atrophy.
    Panigrahi I; Kesari A; Phadke SR; Mittal B
    Neurol India; 2002 Jun; 50(2):117-22. PubMed ID: 12134171
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Barriers and facilitators to clinical trial participation among parents of children with pediatric neuromuscular disorders.
    Peay HL; Biesecker BB; Wilfond BS; Jarecki J; Umstead KL; Escolar DM; Tibben A
    Clin Trials; 2018 Apr; 15(2):139-148. PubMed ID: 29475375
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neuroblastoma in a Patient With Spinal Muscular Atrophy Type I: Is It Just a Coincidence?
    Sag E; Sen HS; Haliloglu G; Yalcin B; Kutluk T
    J Child Neurol; 2015 Jul; 30(8):1075-8. PubMed ID: 25123529
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 'A short time but a lovely little short time': Bereaved parents' experiences of having a child with spinal muscular atrophy type 1.
    Higgs EJ; McClaren BJ; Sahhar MA; Ryan MM; Forbes R
    J Paediatr Child Health; 2016 Jan; 52(1):40-6. PubMed ID: 26437687
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spinal muscular atrophy diagnostics.
    Prior TW
    J Child Neurol; 2007 Aug; 22(8):952-6. PubMed ID: 17761649
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy.
    Wood MF; Hughes SC; Hache LP; Naylor EW; Abdel-Hamid HZ; Barmada MM; Dobrowolski SF; Stickler DE; Clemens PR
    Muscle Nerve; 2014 Jun; 49(6):822-8. PubMed ID: 24307279
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Spinal muscular atrophy in childhood. Possibilities and limits of clinical and molecular genetic diagnosis].
    Zerres K; Rudnik-Schöneborn S; Röhrig D; Wirth B
    Monatsschr Kinderheilkd; 1993 Nov; 141(11):848-54. PubMed ID: 8283989
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [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]  

  • 17. Identifying Opportunities to Provide Family-centered Care for Families With Children With Type 1 Spinal Muscular Atrophy.
    Murrell DV; Crawford CA; Jackson CT; Lotze TE; Wiemann CM
    J Pediatr Nurs; 2018; 43():111-119. PubMed ID: 30266528
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Perspectives on Spinraza (Nusinersen) Treatment Study: Views of Individuals and Parents of Children Diagnosed with Spinal Muscular Atrophy.
    Pacione M; Siskind CE; Day JW; Tabor HK
    J Neuromuscul Dis; 2019; 6(1):119-131. PubMed ID: 30594933
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Synaptic defects in type I spinal muscular atrophy in human development.
    Martínez-Hernández R; Bernal S; Also-Rallo E; Alías L; Barceló MJ; Hereu M; Esquerda JE; Tizzano EF
    J Pathol; 2013 Jan; 229(1):49-61. PubMed ID: 22847626
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.