BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 12861504)

  • 41. [Cystinuria with symptoms of cerebellar atrophy--a case report].
    Tanaka Y; Tsuda M; Miyazaki M; Kuzuhara S
    Rinsho Shinkeigaku; 1991 Mar; 31(3):318-20. PubMed ID: 1893674
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Cerebellar hypoperfusion in infantile neuroaxonal dystrophy.
    Kóbor J; Javaid A; Omojola MF
    Pediatr Neurol; 2005 Feb; 32(2):137-9. PubMed ID: 15664778
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [A patient with an unclassifiable form of neuroaxonal dystrophy].
    Bakker HD; van Gennip AH; Barth PG
    Tijdschr Kindergeneeskd; 1983 Aug; 51(4):147-9. PubMed ID: 6199864
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Infantile neuroaxonal dystrophy].
    Galil A; Schiffmann R; Neeman Z; Porter B
    Harefuah; 1992 Nov; 123(10):387-90, 435. PubMed ID: 1464383
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Duplication of the PLP gene and the classical form of Pelizaeus-Merzbacher disease].
    Blanco-Barca MO; Eirís-Puñal J; Soler-Regal C; Castro-Gago M
    Rev Neurol; 2003 Sep 1-15; 37(5):436-8. PubMed ID: 14533091
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum.
    Sasaki M; Takanashi J; Tada H; Sakuma H; Furushima W; Sato N
    Brain Dev; 2009 Sep; 31(8):582-7. PubMed ID: 18851904
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [The role of electrodiagnostic studies in the diagnosis of hypotonia in infancy].
    Renault F
    Rev Med Liege; 2004; 59 Suppl 1():190-7. PubMed ID: 15244176
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.
    Iannello G; Graziano C; Cenacchi G; Cordelli DM; Zuntini R; Papa V; Magistà AM; Gagliardi M; Procopio R; Quattrone A; Annesi G
    J Neurol Sci; 2017 Oct; 381():209-212. PubMed ID: 28991683
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Infantile neuroaxonal dystrophy--immunohistochemical and ultrastructural studies on the central and peripheral nervous systems in infantile neuroaxonal dystrophy.
    Itoh K; Negishi H; Obayashi C; Hayashi Y; Hanioka K; Imai Y; Itoh H
    Kobe J Med Sci; 1993 Aug; 39(4):133-46. PubMed ID: 8289437
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Superficial siderosis of the central nervous system: an uncommon cause of spastic paraparesia].
    Carod-Artal FJ; Viana-Brandi I; de Melo CM
    Rev Neurol; 2001 Sep 16-30; 33(6):548-52. PubMed ID: 11727238
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Infantile neuroaxonal dystrophy: a rare cause of early childhood ataxia with poor prognosis.
    El Arbi S; Demant A; Kohlschmidt N; Horneff G
    Klin Padiatr; 2013 Jan; 225(1):41-2. PubMed ID: 23073992
    [No Abstract]   [Full Text] [Related]  

  • 52. [Pontocerebellar hypoplasia type 1: a case report].
    Gómez-Lado C; Landín-Iglesias G; Pintos-Martínez E; Pastor-Benavent N; Eirís-Puñal J; Castro-Gago M
    Rev Neurol; 2007 Mar 1-15; 44(5):281-4. PubMed ID: 17342678
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Brain MRI abnormalities in muscular dystrophy due to FKRP mutations.
    Quijano-Roy S; Martí-Carrera I; Makri S; Mayer M; Maugenre S; Richard P; Berard C; Viollet L; Leheup B; Guicheney P; Pinard JM; Estournet B; Carlier RY
    Brain Dev; 2006 May; 28(4):232-42. PubMed ID: 16368217
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis.
    Iodice A; Spagnoli C; Salerno GG; Frattini D; Bertani G; Bergonzini P; Pisani F; Fusco C
    Brain Dev; 2017 Feb; 39(2):93-100. PubMed ID: 27884548
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Ictal and nonictal paroxysmal events in infantile neuroaxonal dystrophy: polygraphic study of a case.
    Santucci M; Ambrosetto G; Scaduto MC; Morbin M; Tzolas EV; Rossi PG
    Epilepsia; 2001 Aug; 42(8):1074-7. PubMed ID: 11554895
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Molecular diagnosis of infantile Neuro axonal Dystrophy by Next Generation Sequencing.
    Goyal M; Bijarnia-Mahay S; Kingsmore S; Farrow E; Saunders C; Saxena R; Verma IC
    Indian J Pediatr; 2015 May; 82(5):474-7. PubMed ID: 25348461
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Early-onset neurodegenerative disease of the cerebellum and motor axons.
    Salman MS; Marles SL; Booth FA; Del Bigio MR
    Pediatr Neurol; 2009 May; 40(5):365-70. PubMed ID: 19380073
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Infantile neuroaxonal dystrophy: axonal changes in biopsied muscle tissue.
    Wakai S; Asanuma H; Tachi N; Ishikawa Y; Minami R
    Pediatr Neurol; 1993; 9(4):309-11. PubMed ID: 8216545
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Multiple symmetric lipomatosis associated to polyneuropathology, atrophy of the cerebellum and mitochondrial cytopathy].
    Castro-Gago M; Alonso A; Pintos-Martínez E; Novo-Rodríguez MI; Blanco-Barca MO; Campos Y; Arenas J; Eirís-Puñal J
    Rev Neurol; 2003 Jun 1-15; 36(11):1026-9. PubMed ID: 12808497
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Cerebellar hypoplasia with heterotopic purkinje cells in the molecular layer and preservation of the granule layers associated with severe encephalopathy. A new entity?
    Pascual-Castroviejo I; Pascual-Pascual SI; Gutierrez-Molina M; Urich H; Katsetos CD
    Neuropediatrics; 2003 Jun; 34(3):160-4. PubMed ID: 12910442
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.