Keyword Analysis & Research: mhbd

az.gov

https://housing.az.gov/manufactured-housing/e-licensing-solution

WEBe-Licensing Solution. We are thrilled to announce the Arizona Manufactured Housing and Building Division’s (MHBD) plan to modernize our licensing and permitting system. This … Location: 602.771.1001

Location: 602.771.1001

DA: 88 PA: 34 MOZ Rank: 23

nature.com

https://www.nature.com/articles/pr2005690

WEBSep 1, 2005 · MHBD is a mitochondrial enzyme that catalyzes the conversion of 2-methyl-3-hydroxybutyryl-CoA to 2-methyl-acetoacetyl-CoA. This disorder is … Author: Celia Perez-Cerda, Judit García-Villoria, Rob Ofman, Pedro Ruiz Sala, Begoña Merinero, Julio Ramos, ... Publish Year: 2005

Author: Celia Perez-Cerda, Judit García-Villoria, Rob Ofman, Pedro Ruiz Sala, Begoña Merinero, Julio Ramos, ...

Publish Year: 2005

DA: 96 PA: 21 MOZ Rank: 31

az.gov

https://housing.az.gov/manufactured-housing/e-licensing-solution

DA: 13 PA: 69 MOZ Rank: 99

wadsworth.org

https://www.wadsworth.org/public-health-programs/newborn-screening/newborn-screening-program/2-methyl-3-hydroxybutyryl-coa-dehydrogenase-deficiency-mhbd

WEBJun 9, 2015 · MHBD deficiency is an inherited metabolic disorder caused by a mutation in the HADH2 gene that affects the breakdown of isoleucine and branched-chain fatty …

DA: 73 PA: 97 MOZ Rank: 52

nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1180283/

WEBApr 14, 2003 · 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency is a novel inborn error of isoleucine degradation. In this article, we report the elucidation of … Author: Rob Ofman, Jos P. N. Ruiter, Marike Feenstra, Marinus Duran, Bwee Tien Poll-The, Johannes Zschocke, ... DOI: 10.1086/375116 Publish Year: 2003 Publication: Am J Hum Genet. 2003 May; 72(5): 1300-1307.

Author: Rob Ofman, Jos P. N. Ruiter, Marike Feenstra, Marinus Duran, Bwee Tien Poll-The, Johannes Zschocke, ...

DOI: 10.1086/375116

Publish Year: 2003

Publication: Am J Hum Genet. 2003 May; 72(5): 1300-1307.

DA: 46 PA: 47 MOZ Rank: 90

sciencedirect.com

https://www.sciencedirect.com/science/article/abs/pii/S0009912008005493

WEBJan 1, 2009 · 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) is a recently described mitochondrial enzyme involved in the degradation pathway of isoleucine and … Author: Judit García-Villoria, Aleix Navarro-Sastre, Carme Fons, Celia Pérez-Cerdá, Antonio Baldellou, Migue... Publish Year: 2009

Author: Judit García-Villoria, Aleix Navarro-Sastre, Carme Fons, Celia Pérez-Cerdá, Antonio Baldellou, Migue...

Publish Year: 2009

DA: 52 PA: 74 MOZ Rank: 4

nature.com

https://www.nature.com/articles/jhg201479

WEBSep 18, 2014 · 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (2M3HBD) deficiency (HSD10 disease) is a rare inborn error of metabolism, and <30 cases have been …

DA: 87 PA: 30 MOZ Rank: 61

nature.com

https://www.nature.com/articles/pr2000286

WEBDec 1, 2000 · In this paper we report the identification of the first patient with a genetic deficiency of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD, EC 1.1.1.178) (2), …

DA: 98 PA: 44 MOZ Rank: 24

springer.com

https://link.springer.com/article/10.1007/s10545-011-9415-4

WEBNov 30, 2011 · HSD10 disease, originally described as 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency and also called 2-methyl-3-hydroxybutyric aciduria, …

DA: 33 PA: 14 MOZ Rank: 81

iomcworld.org

https://www.iomcworld.org/open-access/clinical-diagnosis-and-treatment-of-2methyl3hydroxybutyrylcoa-dehydrogenase-deficiency-in-one-infant-a-case-report-46834.html

WEB2-Methy1-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBDD) is a rare X-linked recessive disorder presenting as the accumulation of 2-methyl-3-hydroxybutyric acid …

DA: 55 PA: 22 MOZ Rank: 64