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 *

262 related articles for article (PubMed ID: 15565656)

  • 21. Hyperargininemia with arginase deficiency.
    Cederbaum SD; Shaw KN; Spector EB; Verity MA; Snodgrass PJ; Sugarman GI
    Pediatr Res; 1979 Jul; 13(7):827-33. PubMed ID: 481955
    [No Abstract]   [Full Text] [Related]  

  • 22. Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes.
    Carvalho DR; Brand GD; Brum JM; Takata RI; Speck-Martins CE; Pratesi R
    Gene; 2012 Nov; 509(1):124-30. PubMed ID: 22959135
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1.
    Mustonen A; Ploos van Amstel HK; Berger R; Salo MK; Viinikka L; Simola KO
    Prenat Diagn; 1997 Oct; 17(10):964-6. PubMed ID: 9358577
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Prenatal gene diagnosis of oculocutaneous albinism type I].
    Li HY; Wu WI; Zheng H; Duan HL; Chen Z; Chen LM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):280-2. PubMed ID: 16767664
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis in maternal plasma of a fetal mutation causing propionic acidemia.
    Bustamante-Aragones A; Pérez-Cerdá C; Pérez B; de Alba MR; Ugarte M; Ramos C
    Mol Genet Metab; 2008; 95(1-2):101-3. PubMed ID: 18599334
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic and biochemical approach to early prenatal diagnosis in a family with mut methylmalonic aciduria.
    Cavicchi C; Donati MA; Funghini S; la Marca G; Malvagia S; Ciani F; Poggi GM; Pasquini E; Zammarchi E; Morrone A
    Clin Genet; 2006 Jan; 69(1):72-6. PubMed ID: 16451139
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of a Japanese family at risk for Tay-Sachs disease. Application of a fluorescent competitive allele-specific polymerase chain reaction (PCR) method.
    Tamasu S; Nishio H; Ayaki H; Lee MJ; Mizutori M; Takeshima Y; Nakamura H; Matsuo M; Maruo T; Sumino K
    Kobe J Med Sci; 1999 Dec; 45(6):259-70. PubMed ID: 10985159
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis using genetic sequencing and identification of a novel mutation in MMACHC.
    Zong Y; Liu N; Zhao Z; Kong X
    BMC Med Genet; 2015 Jul; 16():48. PubMed ID: 26149271
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene.
    Weintrob N; Drouin J; Vallette-Kasic S; Taub E; Marom D; Lebenthal Y; Klinger G; Bron-Harlev E; Shohat M
    Pediatrics; 2006 Feb; 117(2):e322-7. PubMed ID: 16390921
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal diagnosis of beta-thalassemia in Egypt: implementing accurate high-tech methods did not reflect much on the outcome.
    Elgawhary S; Elbaradie Sahar MY; Rashad WM; Mosaad M; Abdalla MA; Ezzat G; Wali YA; Elbeshlawy A
    Pediatr Hematol Oncol; 2008 Sep; 25(6):541-8. PubMed ID: 18728973
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Arginase deficiency, congenital hypothyroidism and hepatic fibrosis].
    Portolés M; Jordá A; Vilas J; García-Piño J
    An Esp Pediatr; 1987 Dec; 27(6):462-6. PubMed ID: 3447498
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of beta-thalassemia in Southern China.
    Li D; Liao C; Li J; Xie X; Huang Y; Zhong H; Wei J
    Eur J Obstet Gynecol Reprod Biol; 2006; 128(1-2):81-5. PubMed ID: 16376479
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Prenatal diagnosis of inborn error of amino acid metabolism].
    Kure S; Tada K
    Nihon Rinsho; 1992 Jul; 50(7):1530-5. PubMed ID: 1404881
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [DNA-based prenatal diagnosis in epidermolysis bullosa].
    Cserhalmi-Friedman BP; Kárpáti S; Horváth A; Tóth T; Tóth-Pál E; Christiano MA
    Orv Hetil; 1998 Jan; 139(2):71-3. PubMed ID: 9451906
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Seven patients of argininemia with spastic tetraplegia as the first and major symptom and prenatal diagnosis of two fetuses with high risk].
    Wu T; Li X; Ding Y; Liu Y; Song J; Wang Q; Li M; Qin Y; Yang Y
    Zhonghua Er Ke Za Zhi; 2015 Jun; 53(6):425-30. PubMed ID: 26310552
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Absence of erythrocyte arginase protein in Japanese patients with hyperargininemia.
    Hayakawa C; Aono S; Keino H; Mizutani N; Watanabe K; Ikemoto M; Totani M; Murachi T; Kashiwamata S
    Eur J Pediatr; 1991 Sep; 150(11):800-3. PubMed ID: 1959545
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of beta-thalassemia in the West Bank and Gaza.
    Ayesh SK; Al-Sharef WA; Nassar SM; Thawabteh NA; Abu-Libdeh BY
    Saudi Med J; 2005 Nov; 26(11):1771-6. PubMed ID: 16311664
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Prenatal gene diagnosis of paternally inherited alpha-thalassemia by detecting fetal DNA in maternal plasma].
    Chen P; Li MJ; Li MQ; Li SQ; Zhou LY; Lin WX
    Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(22):1540-4. PubMed ID: 17785106
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutation analysis and prenatal diagnosis for three families affected by isolated methylmalonic aciduria.
    Kong XD; Shi HR; Liu N; Wu QH; Xu XJ; Zhao ZH; Lu N; Li-Ling J; Luo D
    Genet Mol Res; 2014 Oct; 13(4):8234-40. PubMed ID: 25299208
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism.
    Camire R; Ann Denchy R; Day GA; Lanzano P; Sheth S; Brown S
    Prenat Diagn; 2003 Jun; 23(6):457-60. PubMed ID: 12813758
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.