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 *

62 related articles for article (PubMed ID: 6246834)

  • 1. Chronic Leigh Disease: a genetic and biochemical study.
    Plaitakis A; Whetsell WO; Cooper JR; Yahr MD
    Ann Neurol; 1980 Apr; 7(4):304-10. PubMed ID: 6246834
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Subacute necrotizing encephalomyelopathy (Leigh's disease): clinical and genetic considerations of its adult form.
    Plaitakis A; Whetsell WO; Yahr MD
    Trans Am Neurol Assoc; 1977; 102():32-6. PubMed ID: 210553
    [No Abstract]   [Full Text] [Related]  

  • 3. Leigh syndrome: clinical features and biochemical and DNA abnormalities.
    Rahman S; Blok RB; Dahl HH; Danks DM; Kirby DM; Chow CW; Christodoulou J; Thorburn DR
    Ann Neurol; 1996 Mar; 39(3):343-51. PubMed ID: 8602753
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].
    De Marchi S; Proto G; Jengo A; Collinassi P; Basile A
    Minerva Med; 1983 Feb; 74(7):301-6. PubMed ID: 6828258
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Familial hydrocephalus of prenatal onset.
    Zlotogora J; Sagi M; Cohen T
    Am J Med Genet; 1994 Jan; 49(2):202-4. PubMed ID: 8116668
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Leigh's disease in an adult with evidence of "inhibitor factor" in family members.
    Whetsell WO; Plaitakis A
    Ann Neurol; 1978 Jun; 3(6):519-24. PubMed ID: 209725
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Specificity of the urine inhibitor test for Leigh's disease.
    Pincus JH; Cooper JR; Piros K; Turner V
    Neurology; 1974 Sep; 24(9):885-90. PubMed ID: 4859485
    [No Abstract]   [Full Text] [Related]  

  • 9. [Leigh syndrome in the adult].
    Roquer J; Herraiz J
    Arch Neurobiol (Madr); 1986; 49(3):129-35. PubMed ID: 3017252
    [No Abstract]   [Full Text] [Related]  

  • 10. Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1.
    Blair IP; Gibson RR; Bennett CL; Chance PF
    Am J Med Genet; 2002 Jan; 107(3):190-6. PubMed ID: 11807898
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial auditory neuropathy.
    Wang Q; Gu R; Han D; Yang W
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
    Sobrido MJ; Fernández JM; Fontoira E; Pérez-Sousa C; Cabello A; Castro M; Teijeira S; Alvarez S; Mederer S; Rivas E; Seijo-Martínez M; Navarro C
    Brain; 2005 Jul; 128(Pt 7):1716-27. PubMed ID: 15857933
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cutis laxa of the autosomal recessive type in a consanguineous family.
    de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
    Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cupping.
    Honkanen RA; Jampol LM; Fingert JH; Moore MD; Taylor CM; Stone EM; Alward WL
    Am J Ophthalmol; 2007 May; 143(5):788-794. PubMed ID: 17362864
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kearns-Sayre syndrome.
    Nemet P; Godel V; Lazar M
    Birth Defects Orig Artic Ser; 1982; 18(6):263-8. PubMed ID: 7171761
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.
    Longo I; Scala E; Mari F; Caselli R; Pescucci C; Mencarelli MA; Speciale C; Giani M; Bresin E; Caringella DA; Borochowitz ZU; Siriwardena K; Winship I; Renieri A; Meloni I
    Nephrol Dial Transplant; 2006 Mar; 21(3):665-71. PubMed ID: 16338941
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Subacute necrotizing encephalomyelopathy (Leigh's disease): detection of the heterozygous carrier state.
    Murphy JV
    Pediatrics; 1973 Apr; 51(4):710-5. PubMed ID: 4697519
    [No Abstract]   [Full Text] [Related]  

  • 19. A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism.
    Garcias Gde L; Roth Mda G
    Int J Neurosci; 2007 Jul; 117(7):927-33. PubMed ID: 17613106
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Subacute necrotizing encephalomielopathy. Leigh syndrome (author's transl)].
    Felipe González J; Vargas Torcal F; Loris Pablo C; Borderas F
    An Esp Pediatr; 1978 Mar; 11(3):247-52. PubMed ID: 666130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.