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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 23012868)

  • 21. Abnormal nerve conduction velocity as a marker of immaturity in childhood muscle spinal atrophy.
    Krajewska G; Hausmanowa-Petrusewicz I
    Folia Neuropathol; 2002; 40(2):67-74. PubMed ID: 12230258
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Long-term survival in a child with arthrogryposis multiplex congenita and spinal muscular atrophy.
    Falsaperla R; Romeo G; Di Giorgio A; Pavone P; Parano E; Connolly AM
    J Child Neurol; 2001 Dec; 16(12):934-6. PubMed ID: 11785510
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Progressive spinal amyotrophy type I or Werdnig-Hoffman disease. Apropos of 5 cases in Dakar (Senegal)].
    Ndiaye O; Sall G; Sylla A; Diouf S; Diagne I; Kuakuvi N
    Bull Soc Pathol Exot; 2002 Jun; 95(2):81-2. PubMed ID: 12145964
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Clinical decision making in hypotonia and gross motor delay: a case report of type 1 spinal muscular atrophy in an infant.
    Malerba KH; Tecklin JS
    Phys Ther; 2013 Jun; 93(6):833-41. PubMed ID: 23431212
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Migrating atelectasis in Werdnig-Hoffmann disease: pulmonary manifestations in two cases of spinal muscular atrophy type 1.
    Leistikow EA; Jones NE; Josephson KD; de Sierra TM; Costakos DT; Sprague D; Gorch DH; Asonye UO
    Pediatr Pulmonol; 1999 Aug; 28(2):149-53. PubMed ID: 10423316
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Spinal muscular atrophy in young infants].
    Smit LM; Hageman EG
    Tijdschr Kindergeneeskd; 1989 Jun; 57(3):102-6. PubMed ID: 2799798
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Very severe spinal muscular atrophy--type 0. A cause of congenital multiple arthrogryposis].
    Balslev T; Hertz JM; Rackauskaite G; Sørensen LA
    Ugeskr Laeger; 2001 Oct; 163(41):5679-80. PubMed ID: 11665473
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Atypical presentations of spinal muscular atrophy type III (Kugelberg-Welander disease).
    Kang PB; Krishnamoorthy KS; Jones RM; Shapiro FD; Darras BT
    Neuromuscul Disord; 2006 Aug; 16(8):492-4. PubMed ID: 16797181
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Spinal muscular atrophy associated with olivopontocerebellar hypoplasia. A case report].
    Serra-Ortega A; Torres A; Segreo M
    Rev Neurol; 2005 Jan 16-31; 40(2):90-2. PubMed ID: 15712162
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitochondrial respiratory complex I deficiency simulating spinal muscular atrophy.
    Lee JS; Hwang JS; Ryu KH; Lee EH; Kim SH
    Pediatr Neurol; 2007 Jan; 36(1):45-7. PubMed ID: 17162196
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. Clinical features of spinal muscular atrophy (SMA) type 2.
    Cancès C; Richelme C; Barnerias C; Espil C
    Arch Pediatr; 2020 Dec; 27(7S):7S18-7S22. PubMed ID: 33357592
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Long-term follow-up of a patient with autosomal dominant lower extremity-predominant spinal muscular atrophy-2 due to a BICD2 variant.
    Yamamoto K; Ohashi K; Fujimoto M; Ieda D; Nakamura Y; Hattori A; Kaname T; Ieda K; Nishino I; Saitoh S
    Brain Dev; 2022 Sep; 44(8):578-582. PubMed ID: 35527075
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The test of infant motor performance: reliability in spinal muscular atrophy type I.
    Finkel RS; Hynan LS; Glanzman AM; Owens H; Nelson L; Cone SR; Campbell SK; Iannaccone ST;
    Pediatr Phys Ther; 2008; 20(3):242-6. PubMed ID: 18703961
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Spinal muscular atrophy type I mimicking critical illness neuropathy in a paediatric intensive care neonate: electrophysiological features.
    Fernández-Torre JL; Teja JL; Castellanos A; Figols J; Obeso T; Arteaga R
    Brain Dev; 2008 Oct; 30(9):599-602. PubMed ID: 18384992
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotype and genotype correlation in childhood spinal muscular atrophy.
    Hausmanowa-Petrusewicz I
    Neurol Neurochir Pol; 2001; 35 Suppl 3():29-35. PubMed ID: 12001651
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Respiratory capacity course in patients with infantile spinal muscular atrophy.
    Ioos C; Leclair-Richard D; Mrad S; Barois A; Estournet-Mathiaud B
    Chest; 2004 Sep; 126(3):831-7. PubMed ID: 15364763
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Isolated exon 8 deletion in type 1 spinal muscular atrophy with bilateral optic atrophy: unusual genetic mutation leading to unusual manifestation?
    Maiti D; Bhattacharya M; Yadav S
    J Postgrad Med; 2012; 58(4):294-5. PubMed ID: 23298926
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.