166 related articles for article (PubMed ID: 34991560)
21. Profound neonatal hypoglycemia and lactic acidosis caused by pyridoxine-dependent epilepsy.
Mercimek-Mahmutoglu S; Horvath GA; Coulter-Mackie M; Nelson T; Waters PJ; Sargent M; Struys E; Jakobs C; Stockler-Ipsiroglu S; Connolly MB
Pediatrics; 2012 May; 129(5):e1368-72. PubMed ID: 22529283
[TBL] [Abstract][Full Text] [Related]
22. MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast.
Baruffini E; Dallabona C; Invernizzi F; Yarham JW; Melchionda L; Blakely EL; Lamantea E; Donnini C; Santra S; Vijayaraghavan S; Roper HP; Burlina A; Kopajtich R; Walther A; Strom TM; Haack TB; Prokisch H; Taylor RW; Ferrero I; Zeviani M; Ghezzi D
Hum Mutat; 2013 Nov; 34(11):1501-9. PubMed ID: 23929671
[TBL] [Abstract][Full Text] [Related]
23. A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations.
Shahni R; Wedatilake Y; Cleary MA; Lindley KJ; Sibson KR; Rahman S
Am J Med Genet A; 2013 Sep; 161A(9):2334-8. PubMed ID: 23918765
[TBL] [Abstract][Full Text] [Related]
24. Lactic acidosis, hypotension, and sensorineural hearing loss following intentional metformin overdose.
Miller DK; Brinson AJ; Catalano G; Catalano MC
Curr Drug Saf; 2011 Nov; 6(5):346-9. PubMed ID: 22424544
[TBL] [Abstract][Full Text] [Related]
25. Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7.
Correia SP; Moedas MF; Naess K; Bruhn H; Maffezzini C; Calvo-Garrido J; Lesko N; Wibom R; Schober FA; Jemt A; Stranneheim H; Freyer C; Wedell A; Wredenberg A
Hum Mutat; 2021 Apr; 42(4):378-384. PubMed ID: 33502047
[TBL] [Abstract][Full Text] [Related]
26. Novel pathogenic
Abou Haidar L; Harris RC; Pachnis P; Chen H; Gotway GK; Ni M; DeBerardinis RJ
Cold Spring Harb Mol Case Stud; 2023 Dec; 9(4):. PubMed ID: 37709555
[TBL] [Abstract][Full Text] [Related]
27. Severe lactic acidosis and hypoglycemia due to acute metformin intoxication in a dog.
Ueda Y; Wong C; Borchers A
J Vet Emerg Crit Care (San Antonio); 2018 May; 28(3):274-278. PubMed ID: 29687945
[TBL] [Abstract][Full Text] [Related]
28. A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency.
Oláhová M; Haack TB; Alston CL; Houghton JA; He L; Morris AA; Brown GK; McFarland R; Chrzanowska-Lightowlers ZM; Lightowlers RN; Prokisch H; Taylor RW
Eur J Hum Genet; 2015 Jul; 23(7):935-9. PubMed ID: 25293719
[TBL] [Abstract][Full Text] [Related]
29. Pyruvate dehydrogenase complex deficiency masked by septic shock-induced lactic acidosis: a case report.
Zhou H; Wen Y; Ding H
J Int Med Res; 2024 May; 52(5):3000605241252112. PubMed ID: 38785224
[TBL] [Abstract][Full Text] [Related]
30. A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly.
Jackson CB; Bauer MF; Schaller A; Kotzaeridou U; Ferrarini A; Hahn D; Chehade H; Barbey F; Tran C; Gallati S; Haeberli A; Eggimann S; Bonafé L; Nuoffer JM
Eur J Pediatr; 2016 Apr; 175(4):517-25. PubMed ID: 26563427
[TBL] [Abstract][Full Text] [Related]
31. A Patient with Recurrent Severe Hypoglycemic Attacks and Mitochondrial Complex III Deficiency, Nuclear Type 3: a Novel
Koç Yekedüz M; Öncül Ü; Köse E; Ezgü F; Eminoğlu FT
Mol Syndromol; 2022 Feb; 13(1):64-68. PubMed ID: 35221877
[TBL] [Abstract][Full Text] [Related]
32. A case of hypoglycemia, lactic acidosis, and hematologic malignancy.
Diaz J; Antoine J; Azad N
Endocr Pract; 2010; 16(2):241-3. PubMed ID: 19833585
[TBL] [Abstract][Full Text] [Related]
33. Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: an autosomal recessive syndrome in Persian Jews caused by a mutation in the PUS1 gene.
Zeharia A; Fischel-Ghodsian N; Casas K; Bykhocskaya Y; Tamari H; Lev D; Mimouni M; Lerman-Sagie T
J Child Neurol; 2005 May; 20(5):449-52. PubMed ID: 15971356
[TBL] [Abstract][Full Text] [Related]
34. A unifying diagnosis for pancytopenia, fever, hypoglycemia, and lactic acidosis.
Kloesel B; Vaidya R; Howard MT; Thompson CA
Am J Hematol; 2013 Jan; 88(1):78-81. PubMed ID: 22460726
[No Abstract] [Full Text] [Related]
35. Burkitt's lymphoma presenting with lactic acidosis and hypoglycemia - a case presentation.
Glasheen JJ; Sorensen MD
Leuk Lymphoma; 2005 Feb; 46(2):281-3. PubMed ID: 15621814
[TBL] [Abstract][Full Text] [Related]
36. [
Wang M; Wang DJ; Shu Y; Zhu D; Yu CW; He XY; Zou L
Zhonghua Yu Fang Yi Xue Za Zhi; 2023 Jun; 57(6):912-917. PubMed ID: 37357212
[TBL] [Abstract][Full Text] [Related]
37. Mitochondrial gene sequence variants in children with severe malaria anaemia with or without lactic acidosis: a case control study.
Fowler C; Cserti-Gazdewich C; Dhabangi A; Musoke C; Sharma H; Amr SS; Dzik W
Malar J; 2018 Dec; 17(1):467. PubMed ID: 30545357
[TBL] [Abstract][Full Text] [Related]
38. Non-islet-cell tumor hypoglycemia and lactic acidosis in a child with congenital HIV and Burkitt's lymphoma.
Rastogi MV; Desai N; Quintos JB
J Pediatr Endocrinol Metab; 2008 Aug; 21(8):805-10. PubMed ID: 18825882
[TBL] [Abstract][Full Text] [Related]
39. Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis. An important cause of hypoglycemia in children.
Salih RM; Mohammed EA; Alhashem AM; Mohamed S; Al-Aqeel AI
Saudi Med J; 2020 Feb; 41(2):199-202. PubMed ID: 32020156
[TBL] [Abstract][Full Text] [Related]
40. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
