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: 5611131)

  • 21. [The polycystic kidney and serum alpha-1-antitrypsin deficiency. Observations on 2 family groups].
    Pintacuda S; Di Blasi S; Morici G; Amato S
    Minerva Med; 1981 Jun; 72(26):1697-701. PubMed ID: 6973107
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Hereditary metabolic diseases].
    Odievre M
    Rev Infirm; 1987 Feb; 37(4):14-6. PubMed ID: 3645745
    [No Abstract]   [Full Text] [Related]  

  • 23. [Hereditary metabolic changes in micro-organisms and man. A comparative analysis].
    Brogger A
    Tidsskr Nor Laegeforen; 1968 Sep; 88(18):1659-67. PubMed ID: 5705681
    [No Abstract]   [Full Text] [Related]  

  • 24. Inborn errors of metabolism at the turn of the millennium.
    Barić I; Fumić K; Hoffmann GF
    Croat Med J; 2001 Aug; 42(4):379-83. PubMed ID: 11471189
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Hereditary acatalasemia in dogs].
    Tanase H
    Jikken Dobutsu; 1982 Oct; 31(4):323-5. PubMed ID: 7169091
    [No Abstract]   [Full Text] [Related]  

  • 26. [The need for early treatment of familial inborn errors of iodine metabolism].
    Willgerodt H; Löbe J
    Kinderarztl Prax; 1966 Sep; 34(9):403-14. PubMed ID: 5920402
    [No Abstract]   [Full Text] [Related]  

  • 27. [Sex difference in inborn errors of metabolism and epilepsy].
    Kodama H; Kamoshita S
    No To Shinkei; 1983 Sep; 35(9):877-85. PubMed ID: 6651986
    [No Abstract]   [Full Text] [Related]  

  • 28. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D; Tebib N; Kaabachi N; Ben Dridi MF; Mebazaa A
    Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277
    [No Abstract]   [Full Text] [Related]  

  • 29. Adenine phosphoribosyltransferase deficiency: a previously undescribed genetic defect in man.
    Kelley WN; Levy RI; Rosenbloom FM; Henderson JF; Seegmiller JE
    J Clin Invest; 1968 Oct; 47(10):2281-9. PubMed ID: 5676523
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [New aspects in diagnosis and therapy of hereditary diseases of the nervous and skeletal systems].
    Plecko B; Paschke E
    Wien Klin Wochenschr; 1997 Feb; 109(3):65-7. PubMed ID: 9139463
    [No Abstract]   [Full Text] [Related]  

  • 31. Prominent psychiatric symptoms and glucose hypometabolism in a family with a SNCA duplication.
    Uchiyama T; Ikeuchi T; Ouchi Y; Sakamoto M; Kasuga K; Shiga A; Suzuki M; Ito M; Atsumi T; Shimizu T; Ohashi T
    Neurology; 2008 Oct; 71(16):1289-91. PubMed ID: 18852445
    [No Abstract]   [Full Text] [Related]  

  • 32. Congenital creatine transporter deficiency.
    deGrauw TJ; Salomons GS; Cecil KM; Chuck G; Newmeyer A; Schapiro MB; Jakobs C
    Neuropediatrics; 2002 Oct; 33(5):232-8. PubMed ID: 12536364
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Carnitine transporter deficiency in two Faeroese children].
    Osá E; Simonsen H
    Ugeskr Laeger; 2004 Dec; 166(50):4612-3. PubMed ID: 15633554
    [No Abstract]   [Full Text] [Related]  

  • 34. [Ocular diagnosis in hereditary lysosomal diseases].
    Cantani A; Ciarnella Cantani A; Giardini O; Lendvai D; Santillo C
    Minerva Pediatr; 1980 Nov; 32(22):1283-92. PubMed ID: 7219368
    [No Abstract]   [Full Text] [Related]  

  • 35. [Medium chain Acyl-Coa Dehydrogenase deficiency. A diagnostic challenge for clinicians and laboratory].
    Heinonen OJ; Iitiä A; Irjala K; Pulkki K
    Duodecim; 1996; 112(1):35-41. PubMed ID: 10590599
    [No Abstract]   [Full Text] [Related]  

  • 36. [Familial copper deficiency].
    Petrovicz E; Busa M; Méhes K
    Orv Hetil; 1982 Jul; 123(30):1855-7. PubMed ID: 7133682
    [No Abstract]   [Full Text] [Related]  

  • 37. Prolidase deficiency: case reports of two Argentinian brothers.
    Cabrera HN; Giovanna PD; Bozzini NF; Forlino A
    Int J Dermatol; 2004 Sep; 43(9):684-6. PubMed ID: 15357754
    [No Abstract]   [Full Text] [Related]  

  • 38. Deficiency of lysosomal hydrolases in apparently healthy individuals.
    Zlotogora J; Bach G
    Am J Med Genet; 1983 Jan; 14(1):73-80. PubMed ID: 6131608
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hereditary orotic aciduria. II. A urinary screening test.
    Rogers LE; Porter FS
    Pediatrics; 1968 Sep; 42(3):423-8. PubMed ID: 5677483
    [No Abstract]   [Full Text] [Related]  

  • 40. Red cell enzymopathies as a model of inborn errors of metabolism.
    Miwa S; Kanno H; Hirono A; Fujii H
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088
    [TBL] [Abstract][Full Text] [Related]  

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