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 *

115 related articles for article (PubMed ID: 8011796)

  • 1. [An enteral modular formula in dibasic amino aciduria].
    Serna Juan SA; Sánchez Barroso C; Damas Fernández-Figares M; Valverde Molina E
    Nutr Hosp; 1993; 8(7):441-6. PubMed ID: 8011796
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Renal handling of diamino acids in lysinuric protein intolerance.
    Simell O; Perheentupa J
    J Clin Invest; 1974 Jul; 54(1):9-17. PubMed ID: 4600043
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hazards associated with pregnancies and deliveries in lysinuric protein intolerance.
    Tanner L; Näntö-Salonen K; Niinikoski H; Erkkola R; Huoponen K; Simell O
    Metabolism; 2006 Feb; 55(2):224-31. PubMed ID: 16423630
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hyperdibasicaminoaciduria and hyperammonemia in familial protein intolerance.
    Kato T; Tanaka E; Horisawa S
    Am J Dis Child; 1976 Dec; 130(12):1340-4. PubMed ID: 998577
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria.
    Purkiss P; Chalmers RA; Borud O
    J Inherit Metab Dis; 1980; 3(3):85-6. PubMed ID: 6775144
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline].
    de Parscau L; Vianey-Liaud C; Hermier M; Divry P; Guibaud P
    Arch Fr Pediatr; 1988 Dec; 45(10):809-12. PubMed ID: 3149174
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lysinuric protein intolerance: reviewing concepts on a multisystem disease.
    Sebastio G; Sperandeo MP; Andria G
    Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):54-62. PubMed ID: 21308987
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Intestinal absorption in lysinuric protein intolerance: impaired for diamino acids, normal for citrulline.
    Rajantie J; Simell O; Perheentupa J
    Gut; 1980 Jun; 21(6):519-24. PubMed ID: 6776014
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]].
    Coude FX; Ogier H; Charpentier C; Cathelineau L; Grimber G; Parvy P; Saudubray JM; Frezal J
    Arch Fr Pediatr; 1981 Dec; 38 Suppl 1():829-35. PubMed ID: 6800334
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Excretion of hypusine by children and by patients with familial hyperlysinemia.
    Woody NC; Pupene MB
    Pediatr Res; 1973 Dec; 7(12):994-5. PubMed ID: 4753051
    [No Abstract]   [Full Text] [Related]  

  • 11. Lysinuric protein intolerance.
    Simell O; Perheentupa J; Rapola J; Visakorpi JK; Eskelin LE
    Am J Med; 1975 Aug; 59(2):229-40. PubMed ID: 1155480
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Lysinuric protein intolerance and other cationic aminoacidurias].
    Oyanagi K; Nagao M
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):562-4. PubMed ID: 9645134
    [No Abstract]   [Full Text] [Related]  

  • 13. [Metabolic disorders of branched-chain amino acids: most common forms of organic aciduria in the neonatal period].
    Sperl W; Lehnert W
    Klin Padiatr; 1990; 202(5):334-9. PubMed ID: 2214593
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene.
    Torrents D; Mykkänen J; Pineda M; Feliubadaló L; Estévez R; de Cid R; Sanjurjo P; Zorzano A; Nunes V; Huoponen K; Reinikainen A; Simell O; Savontaus ML; Aula P; Palacín M
    Nat Genet; 1999 Mar; 21(3):293-6. PubMed ID: 10080182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Treatment of organic acidurias and urea cycle disorders.
    Lilliu F
    J Matern Fetal Neonatal Med; 2010 Oct; 23 Suppl 3():73-5. PubMed ID: 20925456
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The dibasic amino acid metabolic disorders].
    Shimizu H
    Nihon Rinsho; 1992 Jul; 50(7):1555-60. PubMed ID: 1404883
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A cluster of lysinuric protein intolerance (LPI) patients in a northern part of Iwate, Japan due to a founder effect. The Mass Screening Group.
    Koizumi A; Shoji Y; Nozaki J; Noguchi A; E X; Dakeishi M; Ohura T; Tsuyoshi K; Yasuhiko W; Manabe M; Takasago Y; Takada G
    Hum Mutat; 2000 Sep; 16(3):270-1. PubMed ID: 10980538
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lysinuric protein intolerance presenting deficiency of argininosuccinate synthetase.
    Ono N; Kishida K; Tokumoto K; Watanabe M; Shimada Y; Yoshinaga J; Fujii M
    Intern Med; 1992 Jan; 31(1):55-9. PubMed ID: 1568044
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families.
    Noguchi A; Shoji Y; Koizumi A; Takahashi T; Matsumori M; Kayo T; Ohata T; Wada Y; Yoshimura I; Maisawa S; Konishi M; Takasago Y; Takada G
    Hum Mutat; 2000; 15(4):367-72. PubMed ID: 10737982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carnitine deficiency and L-carnitine supplementation in lysinuric protein intolerance.
    Tanner LM; Näntö-Salonen K; Rashed MS; Kotilainen S; Aalto M; Venetoklis J; Niinikoski H; Huoponen K; Simell O
    Metabolism; 2008 Apr; 57(4):549-54. PubMed ID: 18328359
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.