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 *

113 related articles for article (PubMed ID: 4841081)

  • 1. Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria.
    Bittles AH; Carson NA
    J Med Genet; 1974 Jun; 11(2):121-2. PubMed ID: 4841081
    [No Abstract]   [Full Text] [Related]  

  • 2. Cystathionase deficiency: evidence for genetic heterogeneity in primary cystathioninuria.
    Pascal TA; Gaull GE; Beratis NG; Gillam BM; Tallan HH
    Pediatr Res; 1978 Feb; 12(2):125-33. PubMed ID: 417288
    [No Abstract]   [Full Text] [Related]  

  • 3. Vitamin B6-responsive and -unresponsive cystathioninuria: two variant molecular forms.
    Pascal TA; Gaull GE; Beratis NG; Gillam BM; Tallan HH; Hirschhorn K
    Science; 1975 Dec; 190(4220):1209-11. PubMed ID: 1198108
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cystathioninuria, renal iminoglycinuria and...alpha 1-antitrypsin...deficiency in the same family: relevance in medical practice.
    Halal F; Scriver CR; Cox DW; Jaber L; Varsano I
    Can Med Assoc J; 1979 Jul; 121(1):64-8. PubMed ID: 313837
    [No Abstract]   [Full Text] [Related]  

  • 5. Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).
    Wang J; Hegele RA
    Hum Genet; 2003 Apr; 112(4):404-8. PubMed ID: 12574942
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cystathioninuria in Down's syndrome.
    Hestnes A; Borud O; Lunde H; Gjessing L
    J Ment Defic Res; 1989 Jun; 33 ( Pt 3)():261-5. PubMed ID: 2526881
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Cystathionuria and defective enzyme regulation].
    Laurent B; Coignet J
    Clin Chim Acta; 1973 Jan; 43(2):171-82. PubMed ID: 4687895
    [No Abstract]   [Full Text] [Related]  

  • 8. [Congenital cystathioninuria. B6-dependent].
    Bravo Mata M; Escribano Rey MD; Alonso Martín A; Alonso Fernández JR
    An Esp Pediatr; 1993 Sep; 39(3):260-4. PubMed ID: 8250445
    [No Abstract]   [Full Text] [Related]  

  • 9. Quantitative analysis of cystathionine and perhydro-1,4-thiazepine-3,5-dicarboxylic acid in the urine of a patient with cystathioninuria using isotachophoresis.
    Kodama H; Sasaki K; Mikasa H; Cavallini D; Ricci G
    J Chromatogr; 1984 Nov; 311(1):183-8. PubMed ID: 6520162
    [No Abstract]   [Full Text] [Related]  

  • 10. Cystathioninuria and homocystinuria.
    Levy HL; Mudd SH; Uhlendorf BW; Madigan PM
    Clin Chim Acta; 1975 Jan; 58(1):51-9. PubMed ID: 1122632
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cystathioninuria].
    Stojanov Lj; Vulović D; Marjanović B; Hajduković R; Zamurović D
    Srp Arh Celok Lek; 1980 Jan; 108(1):41-7. PubMed ID: 7233265
    [No Abstract]   [Full Text] [Related]  

  • 12. Primary cystathioninuria. Methionine load tests and response to pyridoxine.
    Bremer HJ; Endres W
    Helv Paediatr Acta; 1972 Nov; 27(5):525-36. PubMed ID: 4640904
    [No Abstract]   [Full Text] [Related]  

  • 13. Distribution of sulfur in urine of patients with cystathioninuria before and during administration of pyridoxine.
    Frimpter GW; Kozlowski KK; Horwith M
    Metabolism; 1976 Mar; 25(3):355-60. PubMed ID: 1250167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of N-acetyl-S-(3-oxo-3-carboxy-n-propyl)cysteine in the urine of a patient with cystathioninuria using LC/APCI-MS.
    Zhang J; Masuoka N; Ubuka T; Sugahara K; Kodama H
    J Inherit Metab Dis; 1995; 18(6):675-81. PubMed ID: 8750604
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deficiencies of cystathionase and homoserine dehydratase activities in cystathioninuria.
    Finkelstein JD; Mudd SH; Irreverre F; Laster L
    Proc Natl Acad Sci U S A; 1966 Apr; 55(4):865-72. PubMed ID: 5219695
    [No Abstract]   [Full Text] [Related]  

  • 16. Studies with cystathionase-deficient lymphoid cell lines in culture.
    Guarini L; Pascal TA; Gaull GE; Beratis NG
    Enzyme; 1982; 27(2):69-74. PubMed ID: 7073824
    [No Abstract]   [Full Text] [Related]  

  • 17. [Secondary cystathioninuria due to vitamin B 6 deficiency in familial neuroblastoma].
    Plöchl E
    Padiatr Padol; 1976; 11(2-2):444-68. PubMed ID: 967508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Primary, transitory and secondary cystathionineuria].
    Endres W
    Fortschr Med; 1978 May; 96(18):982. PubMed ID: 649003
    [No Abstract]   [Full Text] [Related]  

  • 19. [Various forms of cystathioninuria].
    Endres W
    Fortschr Med; 1982 Mar; 100(11):460-4. PubMed ID: 7076074
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cystathionine synthase deficiency: heterozygote detection using cultured skin fibroblasts.
    Fleisher LD; Tallan HH; Beratis NG; Hirschhorn K; Gaull GE
    Biochem Biophys Res Commun; 1973 Nov; 55(1):38-44. PubMed ID: 4787736
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.