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 *

117 related articles for article (PubMed ID: 6007024)

  • 21. [A case of Albright's dystrophy: "pseudo-pseudo-hypoparathyroidism"].
    de SEZE ; KAHN MF; FRENEAUX B; GRESLE C
    Rev Rhum Mal Osteoartic; 1961 Mar; 28():123-8. PubMed ID: 13750503
    [No Abstract]   [Full Text] [Related]  

  • 22. [Enzymatic disturbances in the urea cycle].
    Colombo JP
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):29-31. PubMed ID: 4098700
    [No Abstract]   [Full Text] [Related]  

  • 23. Corneal erosions in tyrosinosis.
    Zaleski WA; Hill A; Murray RG
    Can J Ophthalmol; 1973 Oct; 8(4):556-9. PubMed ID: 4148055
    [No Abstract]   [Full Text] [Related]  

  • 24. Urinary aminoacids in mental retardation.
    Dhatt PS; Gupta HL; Saini AS
    Indian J Pediatr; 1968 Oct; 35(249):469-75. PubMed ID: 5719650
    [No Abstract]   [Full Text] [Related]  

  • 25. Enzyme defect in saccharopinuria.
    Simell O; Johansson T; Aula P
    J Pediatr; 1973 Jan; 82(1):54-7. PubMed ID: 4404606
    [No Abstract]   [Full Text] [Related]  

  • 26. Hyperprolinaemia in two successive generations of a North American Indian family.
    Perry TL; Hardwick DF; Lowry RB; Hansen S
    Ann Hum Genet; 1968 May; 31(4):401-7. PubMed ID: 4299764
    [No Abstract]   [Full Text] [Related]  

  • 27. [Pathological aminoaciduria in muscular dystrophy].
    Rubio Pérez P; Ramos F; Vivanco F
    Rev Clin Esp; 1972 Sep; 126(6):509-14. PubMed ID: 4658356
    [No Abstract]   [Full Text] [Related]  

  • 28. Alaninuria, associated with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus in two sisters.
    Stimmler L; Jensen N; Toseland P
    Arch Dis Child; 1970 Oct; 45(243):682-5. PubMed ID: 5477682
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Aminoacidpathies of neurological interest].
    Diament AJ
    Arq Neuropsiquiatr; 1974 Jun; 32(2):93-103. PubMed ID: 4848013
    [No Abstract]   [Full Text] [Related]  

  • 30. [Chorio-retinal degenerations and aminoaciduria. III. Atrophia gyrata].
    Rodriguez Caballero ML
    Arch Ophtalmol Rev Gen Ophtalmol; 1975 Dec; 35(12):973-4. PubMed ID: 132162
    [No Abstract]   [Full Text] [Related]  

  • 31. [Aminoaciduria and ocular pathology].
    Ardouin M; Urvoy M; Turquois JP; Chaneac M
    Bull Soc Ophtalmol Fr; 1980; 80(4-5):409-12. PubMed ID: 7460175
    [No Abstract]   [Full Text] [Related]  

  • 32. Hereditary hematuria associated with mental retardation, convulsions, abnormal EEG and ocular abnormalities.
    Hirooka M; Ono T; Kubota N; Yoshioka K; Ikeda S
    Tohoku J Exp Med; 1969 Jun; 98(2):199-211. PubMed ID: 5811104
    [No Abstract]   [Full Text] [Related]  

  • 33. Aminoaciduria in bone diseases in children.
    Opieńska-Blauth J; Gebala A; Sanecka-Obacz M; Kozlowska T; Stryjecka M
    Ann Paediatr; 1966; 207(2):115-24. PubMed ID: 5953604
    [No Abstract]   [Full Text] [Related]  

  • 34. [Enzyme deficiency (disorders of amino acid metabolism, disorders of lipid metabolism)].
    Tsuchida H; Kitabayashi Y; Yamada C; Yokoyama C; Fukui K
    Ryoikibetsu Shokogun Shirizu; 2003; (40):383-6. PubMed ID: 14626144
    [No Abstract]   [Full Text] [Related]  

  • 35. [Chromatographic study of aminoaciduria in subjects with progressive muscular dystrophy and in healthy carriers of such a defect].
    Brunelli B; Falorni A; Cao A; Lungarotti MS; Tangheroni W
    Pediatria (Napoli); 1971; 79(2):168-80. PubMed ID: 5095771
    [No Abstract]   [Full Text] [Related]  

  • 36. Hydroxylysinuria.
    Parker CE; Shaw KN; Jacobs EE; Gutenstein M
    Lancet; 1970 May; 1(7656):1119-20. PubMed ID: 4192000
    [No Abstract]   [Full Text] [Related]  

  • 37. Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population.
    Hyánek J; Homolka J; Seemanová E
    Rev Czech Med; 1974; 20(1):18-22. PubMed ID: 4815837
    [No Abstract]   [Full Text] [Related]  

  • 38. The clinical and biochemical findings in three cases of hypersarcosinemia and one case of transient hypersarcosinuria associated with folic acid deficiency.
    Tippett P; Danks DM
    Helv Paediatr Acta; 1974 Aug; 29(3):261-7. PubMed ID: 4854684
    [No Abstract]   [Full Text] [Related]  

  • 39. Mental retardation due to inborn errors of amino acid metabolism in Puerto Rico. Results of a screening test and a review of other documented cases.
    Crosby PF
    Bol Asoc Med P R; 1971 Jul; 63(7):184-6. PubMed ID: 5286510
    [No Abstract]   [Full Text] [Related]  

  • 40. Hydroxykynureninuria, a case report.
    Jothi A; Seetaram U; Reddy MV; Reddi OS; Reddy PP
    Indian J Pediatr; 1982; 49(399):629-30. PubMed ID: 7152601
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.