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 *

123 related articles for article (PubMed ID: 7619197)

  • 1. Infantile progressive striato-thalamic degeneration in two siblings: a new syndrome.
    Gieron MA; Gilbert-Barness E; Vonsattel JP; Korthals JK
    Pediatr Neurol; 1995 Apr; 12(3):260-3. PubMed ID: 7619197
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.
    Rantamäki M; Krahe R; Paetau A; Cormand B; Mononen I; Udd B
    Neurology; 2001 Sep; 57(6):1043-9. PubMed ID: 11571332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bilateral striatal necrosis, dystonia and optic atrophy in two siblings.
    Leuzzi V; Bertini E; De Negri AM; Gallucci M; Garavaglia B
    J Neurol Neurosurg Psychiatry; 1992 Jan; 55(1):16-9. PubMed ID: 1548491
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive neurodegenerative disorder with trichorrhexis invaginata and ectodermal dysplasia.
    Gyure KA; Kurczynski TW; Gunning W; French BN
    Pediatr Neurol; 1992; 8(6):469-72. PubMed ID: 1476579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial progressive sensorimotor neuropathy with agenesis of the corpus callosum (Andermann syndrome): a clinical, neuroradiological and histopathological study.
    Deleu D; Bamanikar SA; Muirhead D; Louon A
    Eur Neurol; 1997; 37(2):104-9. PubMed ID: 9058066
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Leukoencephalopathy, megalencephaly, and mild clinical course. A recently individualized familial leukodystrophy. Report on five new cases.
    Goutières F; Boulloche J; Bourgeois M; Aicardi J
    J Child Neurol; 1996 Nov; 11(6):439-44. PubMed ID: 9120220
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of infantile neuroaxonal dystrophy and osteopetrosis: a rare autosomal recessive disorder.
    Rees H; Ang LC; Casey R; George DH
    Pediatr Neurosurg; 1995; 22(6):321-7. PubMed ID: 7577667
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal recessive microcephaly with severe psychomotor retardation.
    Scheffer IE; Baraitser M; Wilson J; Godfrey C; Brett EM
    Neuropediatrics; 1992 Feb; 23(1):53-6. PubMed ID: 1565220
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial infantile bilateral striatal necrosis: clinical features and response to biotin treatment.
    Straussberg R; Shorer Z; Weitz R; Basel L; Kornreich L; Corie CI; Harel L; Djaldetti R; Amir J
    Neurology; 2002 Oct; 59(7):983-9. PubMed ID: 12374138
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I; Gutierrez M; Morales C; Gonzalez-Mediero I; Martínez-Bermejo A; Pascual-Pascual SI
    Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Amyotrophic lateral sclerosis: a possible example of autosomal recessive inheritance.
    Della Sala S; Lalatta F; Mazzini L
    Schweiz Arch Neurol Psychiatr (1985); 1991; 142(2):139-47. PubMed ID: 1710388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leber congenital amaurosis in siblings with diffuse dysmyelination.
    Curless RG; Flynn JT; Olsen KR; Post MJ
    Pediatr Neurol; 1991; 7(3):223-5. PubMed ID: 1878105
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Autosomal recessive chorea-acanthocytosis linked to 9q21].
    Requena Caballero I; Arias Gómez M; Lema Devesa C; Sánchez Herrero J; Barros Angueira F; Cotón Vilas JC
    Neurologia; 2000 Mar; 15(3):132-5. PubMed ID: 10846875
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinico-pathological study of a case of familial parkinsonism with striatal degeneration.
    Sakai M; Konagaya M; Kuru S; Kato T; Matsuoka Y; Hashizume Y
    Acta Neuropathol; 2003 Jan; 105(1):76-80. PubMed ID: 12471465
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypertelorism-microtia-clefting (HMC) syndrome.
    Verloes A
    Genet Couns; 1994; 5(3):283-7. PubMed ID: 7811429
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis.
    Sztriha L; Al-Gazali LI; Várady E; Goebel HH; Nork M
    Neuropediatrics; 1999 Jun; 30(3):141-5. PubMed ID: 10480209
    [TBL] [Abstract][Full Text] [Related]  

  • 18. In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.
    Haïk S; Galanaud D; Linguraru MG; Peoc'h K; Privat N; Faucheux BA; Ayache N; Hauw JJ; Dormont D; Brandel JP
    Arch Neurol; 2008 Apr; 65(4):545-9. PubMed ID: 18413481
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Consanguineous marriage and its clinical consequences in migrants to Australia.
    Nelson J; Smith M; Bittles AH
    Clin Genet; 1997 Sep; 52(3):142-6. PubMed ID: 9377802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings.
    Harbord MG; Boyd S; Hall-Craggs MA; Kendall B; McShane MA; Baraitser M
    Neuropediatrics; 1990 Nov; 21(4):218-21. PubMed ID: 2290486
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.