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 *

82 related articles for article (PubMed ID: 5019922)

  • 41. [The so-called brain atrophic process. Clinical introduction and review].
    Joppich G
    Monatsschr Kinderheilkd (1902); 1967 Apr; 115(4):243-7. PubMed ID: 5301921
    [No Abstract]   [Full Text] [Related]  

  • 42. [Normocholesterolemic dyslipoidoses and their otorhinolaryngologic complications].
    Van den Eeckhaut J
    Acta Otorhinolaryngol Belg; 1966; 20(6):657-714. PubMed ID: 5336167
    [No Abstract]   [Full Text] [Related]  

  • 43. [Polyunsaturated Fatty Acid Lipidosis (PFAL). A new disease entity within the concept of amaurotic idiocy and neuronal ceroid lipofuscinosis].
    Hagberg B
    Cesk Neurol Neurochir; 1975 Jun; 38(4):195-201. PubMed ID: 1139701
    [No Abstract]   [Full Text] [Related]  

  • 44. [West's syndrome revealing phacomatosis. Apropos of 2 cases].
    Vaillaud JC; Sabatini R; Sarrouy C
    Presse Med (1893); 1967 Nov; 75(48):2439-42. PubMed ID: 4965380
    [No Abstract]   [Full Text] [Related]  

  • 45. A histological study of the appendix vermiformis. A possible alternative to rectal biopsy in neurological diagnosis.
    Erdohazi M; Read CR
    Dev Med Child Neurol; 1967 Feb; 9(1):98-101. PubMed ID: 6031537
    [No Abstract]   [Full Text] [Related]  

  • 46. [Congenital myopathy with lipid and glycogen overload of muscle fiber and partial deficit of carnitine].
    Gilly R; Carrier H; Lamit J
    Ann Pediatr (Paris); 1980 May; 27(5):319-24. PubMed ID: 6940512
    [No Abstract]   [Full Text] [Related]  

  • 47. [Ocular manifestations of generalized gangliosidosis including the MG 1 (Norman-Landing disease)].
    Seringe P; Dhermy P; Aron JJ
    Arch Ophtalmol Rev Gen Ophtalmol; 1970 Feb; 30(2):113-28. PubMed ID: 4248275
    [No Abstract]   [Full Text] [Related]  

  • 48. Heterozygote detection for autosomal recessive genetic diseases. Community aspects of the Tay-Sachs experience.
    Jackson LG
    Clin Pediatr (Phila); 1974 Apr; 13(4):307-9. PubMed ID: 4821814
    [No Abstract]   [Full Text] [Related]  

  • 49. The differential diagnosis of the various forms of Batten disease by rectal biopsy.
    Lake BD
    Birth Defects Orig Artic Ser; 1976; 12(3):455-62. PubMed ID: 953200
    [No Abstract]   [Full Text] [Related]  

  • 50. [Contribution to the clinical picture and genetics of amaurotic idiocy (late infantile and late forms) with special reference to diagnotic and differential diagnostic problems].
    Bergener M; Jungklaass FK
    Nervenarzt; 1968 Jul; 39(7):316-22. PubMed ID: 5712437
    [No Abstract]   [Full Text] [Related]  

  • 51. [The retina in amaurotic idiocy and tapeto-retinal degenerations].
    Manschot WA
    Ned Tijdschr Geneeskd; 1967 Nov; 111(45):2042-5. PubMed ID: 6064221
    [No Abstract]   [Full Text] [Related]  

  • 52. Sandhoff's disease (GM 2 gangliosidosis type 2): clinical, chemical, and enzyme studies in five patients.
    Okada S; McCrea M; O'Brien JS
    Pediatr Res; 1972 Jul; 6(7):606-15. PubMed ID: 5057290
    [No Abstract]   [Full Text] [Related]  

  • 53. [Eye manifestations in cerebral lipidosis].
    Takeshita K; Kurokawa T; Mitsudome A; Nagayama T
    Ganka; 1969 Aug; 11(8):647-9. PubMed ID: 5391921
    [No Abstract]   [Full Text] [Related]  

  • 54. Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay.
    O'Brien JS; Okada S; Chen A; Fillerup DL
    N Engl J Med; 1970 Jul; 283(1):15-20. PubMed ID: 4986776
    [No Abstract]   [Full Text] [Related]  

  • 55. A case of Wolman's disease.
    Wallis K; Gross M; Kohn R; Zaidman J
    Helv Paediatr Acta; 1971 Apr; 26(1):98-111. PubMed ID: 5577880
    [No Abstract]   [Full Text] [Related]  

  • 56. Ultrastructure of myenteric plexus in lipidoses of children: further approach to a specific diagnosis by rectal biopsy.
    Kamoshita S; Landing BH
    Paediatr Univ Tokyo; 1970 Dec; 18():69-78. PubMed ID: 5514647
    [No Abstract]   [Full Text] [Related]  

  • 57. [Advantage of the skin biopsy in sphingolipidosis and mucopolysaccharidosis in children. A case of Norman-Landing disease with enzyme and ultrastructural study].
    Vissian L; Kermarec J; Manassero J; Duplay H; Vaillaud JC
    Ann Dermatol Syphiligr (Paris); 1970; 97(1):21-38. PubMed ID: 4246037
    [No Abstract]   [Full Text] [Related]  

  • 58. A case of GM2-gangliosidosis with total hexosaminidase deficiency.
    Suzuki Y; Jacob JC; Suzuki K; Suzuki K
    Neurology; 1970 Apr; 20(4):388. PubMed ID: 5535009
    [No Abstract]   [Full Text] [Related]  

  • 59. [Xanthomatosis as one of the manifestations of lipidoses].
    Kustova NI; Soskin IaM; Emel'ianov AM
    Klin Med (Mosk); 1984 Apr; 62(4):132-5. PubMed ID: 6737962
    [No Abstract]   [Full Text] [Related]  

  • 60. Farber's lipogranulomatosis.
    Vaidya VU; Bharucha BA; Kagalwala TY; Pandya AL; Kumta NB
    Indian Pediatr; 1987 Aug; 24(8):673-5. PubMed ID: 3327826
    [No Abstract]   [Full Text] [Related]  

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