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 *

128 related articles for article (PubMed ID: 38146578)

  • 41. Involvement of erythrocyte calpain in glycine- and carnitine-treated isovaleric acidemia.
    Salamino F; Di Lisa F; Burlina AB; Menabŏ R; Barbato R; De Tullio R; Siliprandi N
    Pediatr Res; 1994 Aug; 36(2):182-6. PubMed ID: 7970932
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Selective and accurate C5 acylcarnitine quantitation by UHPLC-MS/MS: Distinguishing true isovaleric acidemia from pivalate derived interference.
    Minkler PE; Stoll MSK; Ingalls ST; Hoppel CL
    J Chromatogr B Analyt Technol Biomed Life Sci; 2017 Sep; 1061-1062():128-133. PubMed ID: 28734160
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Isovaleryl-CoA dehydrogenase activity in isovaleric acidemia fibroblasts using an improved tritium release assay.
    Hyman DB; Tanaka K
    Pediatr Res; 1986 Jan; 20(1):59-61. PubMed ID: 3753755
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia.
    Vatanavicharn N; Liammongkolkul S; Sakamoto O; Sathienkijkanchai A; Wasant P
    Pediatr Int; 2011 Dec; 53(6):990-4. PubMed ID: 22004070
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Changing plasma and urinary organic acid levels in a patient with isovaleric acidemia during an attack.
    Shigematsu Y; Sudo M; Momoi T; Inoue Y; Suzuki Y; Kameyama J
    Pediatr Res; 1982 Sep; 16(9):771-5. PubMed ID: 7133811
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Phenotypic Variability and Newly Identified Mutations of the IVD Gene in Japanese Patients with Isovaleric Acidemia.
    Sakamoto O; Arai-Ichinoi N; Mitsubuchi H; Chinen Y; Haruna H; Maruyama H; Sugawara H; Kure S
    Tohoku J Exp Med; 2015 Jun; 236(2):103-6. PubMed ID: 26018748
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The glycine
    Kühn S; Williams ME; Dercksen M; Sass JO; van der Sluis R
    Comput Struct Biotechnol J; 2023; 21():1236-1248. PubMed ID: 36817957
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Isovaleric acidemia with promyelocytic myeloproliferative syndrome.
    Gilbert-Barness E; Barness LA
    Pediatr Dev Pathol; 1999; 2(3):286-91. PubMed ID: 10191353
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Atypical MR lenticular signal change in infantile isovaleric acidemia.
    Wani NA; Qureshi UA; Jehangir M; Ahmad K; Hussain Z
    Indian J Radiol Imaging; 2016; 26(1):131-4. PubMed ID: 27081237
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Useful second-tier tests in expanded newborn screening of isovaleric acidemia and methylmalonic aciduria.
    Shigematsu Y; Hata I; Tajima G
    J Inherit Metab Dis; 2010 Oct; 33(Suppl 2):S283-8. PubMed ID: 20440648
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Isovaleric acidemia. Clinical presentation of 6 cases.
    Tokatli A; Coşkun T; Ozalp I
    Turk J Pediatr; 1998; 40(1):111-9. PubMed ID: 9673537
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Genetic mutation profile of isovaleric acidemia patients in Taiwan.
    Lin WD; Wang CH; Lee CC; Lai CC; Tsai Y; Tsai FJ
    Mol Genet Metab; 2007 Feb; 90(2):134-9. PubMed ID: 17027310
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Isovaleric aciduria identified by newborn screening: Strategies to predict disease severity and stratify treatment.
    Mütze U; Henze L; Schröter J; Gleich F; Lindner M; Grünert SC; Spiekerkoetter U; Santer R; Thimm E; Ensenauer R; Weigel J; Beblo S; Arélin M; Hennermann JB; Marquardt I; Freisinger P; Krämer J; Dieckmann A; Weinhold N; Schiergens KA; Maier EM; Hoffmann GF; Garbade SF; Kölker S
    J Inherit Metab Dis; 2023 Nov; 46(6):1063-1077. PubMed ID: 37429829
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Intravenous L-carnitine and acetyl-L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiency and isovaleric acidemia.
    Van Hove JL; Kahler SG; Millington DS; Roe DS; Chace DH; Heales SJ; Roe CR
    Pediatr Res; 1994 Jan; 35(1):96-101. PubMed ID: 8134205
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Endogenous catabolism is the major source of toxic metabolites in isovaleric acidemia.
    Millington DS; Roe CR; Maltby DA; Inoue F
    J Pediatr; 1987 Jan; 110(1):56-60. PubMed ID: 3794887
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A Case Report of a Novel Isovaleryl-CoA Dehydrogenase Gene Mutation in a Chinese Family with Isovaleric Acidemia.
    Chen W; Miao C; Li Y; Wang X; Wu W; Long Q; Jiang Y; Yan Z; Cui Y
    Clin Lab; 2023 Sep; 69(9):. PubMed ID: 37702673
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Acute and chronic-intermittent isovaleric acidemia: diagnosis and glycine therapy.
    Elsas LJ; Naglak M
    Acta Paediatr Jpn; 1988 Aug; 30(4):442-51. PubMed ID: 3150234
    [No Abstract]   [Full Text] [Related]  

  • 58. Newborn screening for isovaleric acidemia in Quanzhou, China.
    Lin Y; Chen D; Peng W; Wang K; Lin W; Zhuang J; Zheng Z; Li M; Fu Q
    Clin Chim Acta; 2020 Oct; 509():25-29. PubMed ID: 32505769
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Isovaleric acidemia due to compound heterozygous variants of IVD gene in a case].
    Che F; Yang Y; Wang Z; Wang G; Wu H; Zhang L; Wei J; Zhao Y; Zhao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Feb; 38(2):150-153. PubMed ID: 33565069
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Acute decompensation of isovaleric acidemia induced by Graves' disease.
    Kimmoun A; Abboud G; Strazeck J; Merten M; Guéant JL; Feillet F
    Intensive Care Med; 2008 Dec; 34(12):2315-6. PubMed ID: 18607566
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.