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 *

184 related articles for article (PubMed ID: 14081787)

  • 21. [FAMILIAL PROGRESSIVE CHRONIC BULBOPONTINE PARALYSIS WITH DEAFNESS. A CASE OF KLIPPEL-TRENAUNAY'S SYNDROME IN THE SAME FAMILY. DIAGNOSTIC PROBLEMS. REMARKS ON HEREDITY].
    VANLAERE J
    Verh K Vlaam Acad Geneeskd Belg; 1964; 26():189-253. PubMed ID: 14162264
    [No Abstract]   [Full Text] [Related]  

  • 22. [On the syndrome: ichthyosis congenita, feeblemindedness and spastic disorders of the type of Little's disease].
    GREITHER A
    Hautarzt; 1959 Sep; 10():403-8. PubMed ID: 13851752
    [No Abstract]   [Full Text] [Related]  

  • 23. An X-linked syndrome with microcephaly, severe mental retardation, spasticity, epilepsy and deafness.
    Renier WO; Gabreëls FJ; Jasper HH; Hustinx TW; Geelen JA; van Haelst UJ
    J Ment Defic Res; 1982 Mar; 26(Pt 1):27-40. PubMed ID: 7077653
    [No Abstract]   [Full Text] [Related]  

  • 24. Zinc and copper concentration in serum of patients with congenital ichthyosis, spastic di- or tetraplegia and mental retardation (Sjögren-Larsson syndrome).
    Jagell S; Hallmans G; Gustavson KH
    Ups J Med Sci; 1981; 86(3):291-5. PubMed ID: 7324288
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spastic quadriplegia combined with congenital ichthyosiform erythroderma and oligophrenia.
    BLUMEL J; WATKINS M; EGGERS GW
    AMA J Dis Child; 1958 Dec; 96(6):724-6. PubMed ID: 13594021
    [No Abstract]   [Full Text] [Related]  

  • 26. On the diagnosis of syndromes in mental retardation.
    Garrard SD
    Pediatr Clin North Am; 1968 Nov; 15(4):925-42. PubMed ID: 4236263
    [No Abstract]   [Full Text] [Related]  

  • 27. Oligophrenia combined with congenital ichthyosiform erythrodermia, spastic syndrome and macularretinal degeneration; a clinical and genetic study.
    SJOGREN T
    Acta Genet Stat Med; 1956; 6(1 Part 2):80-91. PubMed ID: 13354244
    [No Abstract]   [Full Text] [Related]  

  • 28. [GENETIC MENTAL DEFICIENCY].
    NODOT A
    Rev Neuropsychiatr Infant; 1963; 11():433-46. PubMed ID: 14200146
    [No Abstract]   [Full Text] [Related]  

  • 29. [THE XXXXY SYNDROME].
    PRADER A; MUERSET G; HAUSCHTECK E
    Arch Kinderheilkd; 1964 Feb; 170():20-33. PubMed ID: 14163925
    [No Abstract]   [Full Text] [Related]  

  • 30. A FAMILY WITH HEREDITARY SPASTIC ATAXIA: AN INVESTIGATION INTO THE EXISTENCE OF THE SO CALLED "FORMES FRUSTES".
    van Beusekom ; Staal A; Went LN
    Acta Neurol Scand; 1965; 41(2):97-119. PubMed ID: 14289917
    [No Abstract]   [Full Text] [Related]  

  • 31. [Oligophrenia, spasmodic paraplegia (Little type) and congenital ichthyosis in a little premature girl. Sjoegren-Larsson synkrome].
    SCHACHTER M
    Acta Pediatr Esp; 1961 Mar; 19():195-9. PubMed ID: 13747142
    [No Abstract]   [Full Text] [Related]  

  • 32. [RECENT RESULTS OF MEDICAL GENETICS, ESPECIALLY IN THE NEUROPSYCHIATRIC SECTOR].
    HABERLANDT WF
    Wien Klin Wochenschr; 1964 Mar; 76():165-70. PubMed ID: 14186560
    [No Abstract]   [Full Text] [Related]  

  • 33. A syndrome of retinitis pigmentosa, congenital ichthyosis, hypergonadotropic hypogonadism, small stature, mental retardation, cranial dysmorphism, and abnormal electroencephalogram.
    Kaufman LM
    Ophthalmic Genet; 1998 Jun; 19(2):69-79. PubMed ID: 9695088
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [ON THE CAUSES OF CONGENITAL MENTAL DEFICIENCY].
    ARIMA M; KOMIYA K; NAKAGOME Y
    Seishin Igaku; 1963 Oct; 5():763-77. PubMed ID: 14092562
    [No Abstract]   [Full Text] [Related]  

  • 35. The Rud syndrome: ichthyosis, hypogonadism, mental retardation.
    Nissley PS; Thomas GH
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):246-7. PubMed ID: 5173271
    [No Abstract]   [Full Text] [Related]  

  • 36. [Clinical symptomatology and diagnostic criteria in Rud's syndrome].
    Ignatowicz R; Michałowicz R; Kubicka K; Kmieć T; Jóźwiak S
    Pol Tyg Lek; 1985 Dec; 40(49):1374-5. PubMed ID: 3831985
    [No Abstract]   [Full Text] [Related]  

  • 37. GEOGRAPHICAL DISTRIBUTION OF SOME ISOLATES WITH NEURO-GENETICAL AFFECTIONS IN SWITZERLAND.
    KLEIN D; AMMANN F
    J Genet Hum; 1964; 13():122-32. PubMed ID: 14192059
    [No Abstract]   [Full Text] [Related]  

  • 38. [HYPERTELORISM AND LISSENCEPHALIA. STUDY OF A FAMILIAL FORM (FAMILY MA..). (PRELIMINARY REPORT)].
    REZNIK M; ALBERCA RS
    Acta Neurol Psychiatr Belg; 1963 Nov; 63():970-3. PubMed ID: 14096303
    [No Abstract]   [Full Text] [Related]  

  • 39. RESEARCH INTO MENTAL SUBNORMALITY. 2. BIOCHEMICAL DISORDERS AND MENTAL RETARDATION.
    GIBSON J
    Nurs Times; 1964 May; 60():624-5. PubMed ID: 14147186
    [No Abstract]   [Full Text] [Related]  

  • 40. WAARDENBERG SYNDROME. A STUDY OF A FAMILY WITH ONE CHILD MANIFESTING ALL THE CHARACTERISTICS.
    KATTULA S
    J Otolaryngol Soc Aust; 1964 Sep; 1():307-12. PubMed ID: 14234131
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.