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 *

57 related articles for article (PubMed ID: 5360831)

  • 21. [Disorders of amino acids metabolism in Marinesco-Sjögren syndrom].
    Biesold D; Markwardt H
    Padiatr Grenzgeb; 1968; 7(2):135-9. PubMed ID: 5716358
    [No Abstract]   [Full Text] [Related]  

  • 22. Congenital cataract, ataxia, external ophthalmoplegia and dysphagia in two siblings. A Marinesco-Sjögren-like syndrome.
    Schulz S; Vielhaber S; Muschke P; Mohnike K; Gooding R; Wieacker P
    Neuropediatrics; 2007 Apr; 38(2):88-90. PubMed ID: 17712737
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31.
    Lagier-Tourenne C; Tranebaerg L; Chaigne D; Gribaa M; Dollfus H; Silvestri G; Bétard C; Warter JM; Koenig M
    Eur J Hum Genet; 2003 Oct; 11(10):770-8. PubMed ID: 14512967
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Marinescu-Sjögren-Garland syndrome (with reference to 2 familial cases)].
    Lupu IM; Părău T; Rebega M
    Pediatria (Bucur); 1969; 18(2):149-55. PubMed ID: 5374909
    [No Abstract]   [Full Text] [Related]  

  • 25. [Sjögren-Larsson syndrome. Study of 2 cases].
    Cabezuelo-Huerta G; Mulas F; Frontera-Izquierdo P
    An Esp Pediatr; 1983 May; 18(5):399-402. PubMed ID: 6614675
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A new case of Martsolf syndrome.
    Bora E; Cankaya T; Alpman A; Karaca E; Cogulu O; Tekgul H; Ozkinay F
    Genet Couns; 2007; 18(1):71-5. PubMed ID: 17515302
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Oligophrenia, cerebellar ataxia and cataract; the syndrome of Marinesco-Garland.
    MACGILLIVRAY RC
    Am J Ment Defic; 1957 Apr; 61(4):719-24. PubMed ID: 13410986
    [No Abstract]   [Full Text] [Related]  

  • 28. Orthopaedic manifestations of Marinesco-Sjögren syndrome.
    Reinker K; Hsia YE; Rimoin DL; Henry G; Yuen J; Powell B; Wilcox WR
    J Pediatr Orthop; 2002; 22(3):399-403. PubMed ID: 11961464
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Marinesco-Sjögren syndrome with chronic progressive ophthalmoplegia caused by presumed defective oxidative phosphorylation].
    Berio A; Piazzi A
    Pediatr Med Chir; 1996; 18(1):99-103. PubMed ID: 8685033
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Pigmentary retinal degeneration, mental deterioration and ataxia: Stewart's Syndrome ].
    Calatayud T; Campos-Castello J; Negrete O; Careaga J
    Arch Neurobiol (Madr); 1982; 45(3):205-12. PubMed ID: 7125810
    [No Abstract]   [Full Text] [Related]  

  • 31. Marinesco-Sjogren syndrome: can the diagnosis be made prior to cataract formation?
    Shimizu T; Matsuishi T; Yamashita Y; Koga Y; Ohtaki E; Kato H; Goto Y; Nonaka I
    Muscle Nerve; 1997 Jul; 20(7):909-10. PubMed ID: 9179171
    [No Abstract]   [Full Text] [Related]  

  • 32. [Torsten-Sjögren syndrome].
    Rister M; Rudolph W; Lemmen K; Konen W
    Monatsschr Kinderheilkd; 1984 Mar; 132(3):180-1. PubMed ID: 6727891
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Demographic factors affect the occurrence of severe mental retardation. Is intermarriage a factor of significance also in Sweden?].
    Fernell E
    Lakartidningen; 1998 Aug; 95(35):3663-6. PubMed ID: 9748778
    [No Abstract]   [Full Text] [Related]  

  • 34. Sjögren-Larsson syndrome: Indian and Central European similarities.
    Möhrenschlager M; Braun-Falco M; Ring J
    Pediatr Dermatol; 2005; 22(6):574-5. PubMed ID: 16354271
    [No Abstract]   [Full Text] [Related]  

  • 35. 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]  

  • 36. [Sjögren-Larsson syndrome].
    Vajda P; Brozmanová M; Szabová I
    Cesk Pediatr; 1982 Jun; 37(6):329-30. PubMed ID: 7105232
    [No Abstract]   [Full Text] [Related]  

  • 37. Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
    Mégarbané A; Choueiri R; Bleik J; Mezzina M; Caillaud C
    J Med Genet; 1999 Aug; 36(8):637-40. PubMed ID: 10465117
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rapid cataract formation in Marinesco-Sjögren syndrome.
    Ishikawa T; Kitoh H; Awaya A; Nonaka I
    Pediatr Neurol; 1993; 9(5):407-8. PubMed ID: 8292220
    [No Abstract]   [Full Text] [Related]  

  • 39. [Sjögren-Larsen syndrome].
    Szliwowski HB; Henry J; Pelc S
    Acta Paediatr Belg; 1967; 21(2):125-32. PubMed ID: 5595212
    [No Abstract]   [Full Text] [Related]  

  • 40. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R
    Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 3.