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 *

50 related articles for article (PubMed ID: 5749398)

  • 1. [Congenital malformations, with special reference to clinicopathological studies].
    Hamada S
    Shinkei Kenkyu No Shimpo; 1968; 12(1):227-41. PubMed ID: 5749398
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Hereditary paroxysmal ataxia with mental retardation: a clinicopathological study in relation to episodic ataxia type 2.
    Mochizuki Y; Kawata A; Mizutani T; Takamoto K; Hayashi H; Taki K; Morimatsu Y
    Acta Neuropathol; 2004 Oct; 108(4):345-9. PubMed ID: 15300451
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Morphological aspects of mental retardation.
    Crome L
    Proc R Soc Med; 1972 Jul; 65(7):587-8. PubMed ID: 5085929
    [No Abstract]   [Full Text] [Related]  

  • 5. [A pathological study on patients with severe physical and mental disturbances, with special reference to the relationship with clinical observations].
    Murofushi K; Morimatsu Y; Handa T; Shinohara T
    Seishin Shinkeigaku Zasshi; 1971 Feb; 73(2):136-50. PubMed ID: 4252195
    [No Abstract]   [Full Text] [Related]  

  • 6. New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
    Yanagisawa A; Bouchet C; Van den Bergh PY; Cuisset JM; Viollet L; Leturcq F; Romero NB; Quijano-Roy S; Fardeau M; Seta N; Guicheney P
    Neurology; 2007 Sep; 69(12):1254-60. PubMed ID: 17634419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases].
    Campistol Plana J; Arellano Pedrola M; Poo Argüelles P; Escofet Sotera C; Pérez Olarte P; Vilaseca Buscà MA
    An Esp Pediatr; 1999 Aug; 51(2):139-42. PubMed ID: 10495499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M; Sugio Y
    J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mental handicap: the hidden handicap factors.
    Cowie V
    Nurs Mirror; 1980 Jan; 152(5):36-7. PubMed ID: 6906804
    [No Abstract]   [Full Text] [Related]  

  • 10. [Central nervous system lesions in cytomegalic disease].
    Autelitano F; Piccardo V
    Recenti Prog Med; 1981 Oct; 71(4):343-80. PubMed ID: 6278549
    [No Abstract]   [Full Text] [Related]  

  • 11. Rhombencephalosynapsis with and without associated malformations.
    Jellinger KA
    Acta Neuropathol; 2009 Feb; 117(2):219. PubMed ID: 19137321
    [No Abstract]   [Full Text] [Related]  

  • 12. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
    Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
    BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome.
    Majewski F; Goecke T
    Am J Med Genet; 1982 May; 12(1):7-21. PubMed ID: 7046443
    [No Abstract]   [Full Text] [Related]  

  • 14. Congenital malformations in offspring of phenylketonuric mothers.
    Stevenson RE; Huntley CC
    Pediatrics; 1967 Jul; 40(1):33-45. PubMed ID: 6028897
    [No Abstract]   [Full Text] [Related]  

  • 15. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M; Ito M; Hall BD
    Am J Med Genet; 1984 Jan; 17(1):367-74. PubMed ID: 6711604
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new case of Balci's syndrome (corneal opacity, microphthalmia, microcephaly, mental retardation, and generalized muscular spasticity associated with congenital heart disease).
    Balci S; Demirçeken FG; Ocal B; Zorlu P; Teziç T
    Turk J Pediatr; 2001; 43(4):366-8. PubMed ID: 11765173
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Neuronal migration disorders. Radiological and clinical aspects].
    Orderud WJ; Skjeldal OH; Strømme P
    Tidsskr Nor Laegeforen; 1995 Jun; 115(16):1952-6. PubMed ID: 7638849
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonspecific mental retardation in British Columbia as ascertained through a registry.
    Herbst DS; Baird PA
    Am J Ment Defic; 1983 Mar; 87(5):506-13. PubMed ID: 6837641
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic correlations of ocular coloboma without known cause.
    Leppig KA; Pagon RA
    Clin Dysmorphol; 1993 Oct; 2(4):322-31. PubMed ID: 8305963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
    Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E
    Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.