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 *

89 related articles for article (PubMed ID: 1134937)

  • 41. A Turkish case of subcortical/subependymal heterotopia associated with corpus callosum dysgenesis, craniofacial dysmorphism, severe eye abnormalities, and growth-mental retardation.
    Caksen H; Tuncer O; Ataş B; Demirok A; Unal O; Ikbal M; Odabaş D
    Genet Couns; 2003; 14(3):343-8. PubMed ID: 14577680
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Visceral leishmaniasis. Practical considerations on a clinical case].
    Ronconi GF; Gualandi V; Bertoli GL; Ronconi M; Valli F
    Pediatr Med Chir; 1984; 6(4):575-7. PubMed ID: 6533607
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Short stature, mental retardation and ocular alterations in three siblings.
    Mollica F; Pavone L; Antener I
    Helv Paediatr Acta; 1972 Nov; 27(5):463-9. PubMed ID: 4640901
    [No Abstract]   [Full Text] [Related]  

  • 44. [Familial lymphohistiocytosis: a report of three cases with general review. Possible links with secondary syndromes (author's transl)].
    Nèzelof C; Eliachar E
    Nouv Rev Fr Hematol; 1973; 13(3):319-37. PubMed ID: 4270586
    [No Abstract]   [Full Text] [Related]  

  • 45. Letter: Parenteral copper in Menkes' kinky-hair syndrome.
    Garnica AD; Fletcher SR
    Lancet; 1975 Oct; 2(7936):659-60. PubMed ID: 52027
    [No Abstract]   [Full Text] [Related]  

  • 46. [Case of Lowe's syndrome in an infant].
    Nizankowska-Blaz T
    Wiad Lek; 1971 May; 24(9):875-7. PubMed ID: 5579365
    [No Abstract]   [Full Text] [Related]  

  • 47. [Modern trends in inborn errors of metabolism (reports) (author's transl)].
    Bickel H; Molz G
    Verh Dtsch Ges Pathol; 1971; 55():356-75. PubMed ID: 4130732
    [No Abstract]   [Full Text] [Related]  

  • 48. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS; Wisniewski K; Brown WT
    Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Sex-linked neurodegenerative disease associated with monilethrix.
    Bray PF
    Pediatrics; 1965 Sep; 36(3):417-20. PubMed ID: 5829335
    [No Abstract]   [Full Text] [Related]  

  • 50. [Oculo-cerebro-renal syndrome (Lowe's syndrome): clinical study of a case].
    Massicotte P; Robillard J; Guay M; Laverdière M; Lapierre JG
    Union Med Can; 1971 Jun; 100(6):1136-47. PubMed ID: 5561238
    [No Abstract]   [Full Text] [Related]  

  • 51. [Lowe's syndrome. Study of a case].
    Junco E; Rodrigo F; Pascual Castroviejo I
    Arch Neurobiol (Madr); 1972; 35(2):119-32. PubMed ID: 5025358
    [No Abstract]   [Full Text] [Related]  

  • 52. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
    Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH
    Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A new X-linked mental retardation-overgrowth syndrome.
    Golabi M; Rosen L
    Am J Med Genet; 1984 Jan; 17(1):345-58. PubMed ID: 6538755
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [A case of Lowe's syndrome].
    Ardouin M; Catros A; Lemarrec B; Belloir D; Chanteau Y; Chauvel A
    Bull Soc Ophtalmol Fr; 1971; 71(7):816-8. PubMed ID: 5144806
    [No Abstract]   [Full Text] [Related]  

  • 55. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L; El-Nabi MM; Azab AS; Gouda SA; Al-Wadaani AM; Naguib KK
    East Mediterr Health J; 2007; 13(4):975-9. PubMed ID: 17955782
    [No Abstract]   [Full Text] [Related]  

  • 56. Menkes' kinky-hair syndrome.
    Danks DM; Campbell PE; Walker-Smith J; Stevens BJ; Gillespie JM; Blomfield J; Turner B
    Lancet; 1972 May; 1(7760):1100-2. PubMed ID: 4112576
    [No Abstract]   [Full Text] [Related]  

  • 57. [Neuropathology of Lowe's syndrome and of oculo-cerebro-renal syndromes].
    Tommasi M; Tabib A; Gilly J; Jeune M; Patricot LM
    Lyon Med; 1971 Dec; 226(19):719-23. PubMed ID: 5159269
    [No Abstract]   [Full Text] [Related]  

  • 58. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ
    Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Menkes disease. (A family case report)].
    Tilmont P; Louis J; Blanckaert D; Martin JJ; Morel P; Dubois B; Farriaux JP; Fontaine G
    Ann Pediatr (Paris); 1978 Sep; 25(7):333-40. PubMed ID: 16114343
    [No Abstract]   [Full Text] [Related]  

  • 60. [Neuropathology of trichopoliodystrophy (Menkes' disease). Anatomoclinical observation].
    Kopp N; Tommasi M; Carrier H; Pialat J; Gilly J; Herve C
    Rev Neurol (Paris); 1975 Nov; 131(11):775-89. PubMed ID: 1221486
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.