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Longer titles found: Primary hyperoxaluria (view)

searching for Hyperoxaluria 14 found (51 total)

Livedo reticularis (2,547 words) [view diff] exact match in snippet view article find links to article

facial dysmorphism, immunodeficiency, livedo, and short stature) Primary hyperoxaluria, oxalosis (oxalate vasculopathy) Cytomegalovirus infection (very rare

Oxalobacter formigenes (2,825 words) [view diff] exact match in snippet view article find links to article

Oxalobacter formigenes in cystic fibrosis patients: a risk factor for hyperoxaluria". Lancet. 352 (9133): 1026–1029. doi:10.1016/S0140-6736(98)03038-4.

Peroxisomal disorder (578 words) [view diff] exact match in snippet view article find links to article

Pipecolic acidemia 600964 PHYH E80.301 Acatalasia 115500 CAT E80.310 Hyperoxaluria type 1 259900 AGXT E80.311 Acyl-CoA oxidase deficiency 264470 ACOX1

Oxalic acid (4,104 words) [view diff] exact match in snippet view article find links to article

Rhubarb Compendium) Oxalosis & Hyperoxaluria Foundation (OHF) The Oxalate Content of Food 2008 (PDF) Oxalosis & Hyperoxaluria Foundation (OHF) Diet Information

AGXT2 (455 words) [view diff] exact match in snippet view article find links to article

1152/ajpcell.00238.2004. PMID 15240345. Danpure CJ (August 2005). "Primary hyperoxaluria: from gene defects to designer drugs?". Nephrology, Dialysis, Transplantation

Hydroxyacid oxidase (glycolate oxidase) 1 (614 words) [view diff] exact match in snippet view article

1016/j.abb.2007.06.021. PMID 17669354. Danpure CJ (2005). "Primary hyperoxaluria: From gene defects to designer drugs?". Nephrology Dialysis Transplantation

List of MeSH codes (C12) (1,422 words) [view diff] exact match in snippet view article

syndrome MeSH C12.777.419.307 – hydronephrosis MeSH C12.777.419.320 – hyperoxaluria, primary MeSH C12.777.419.331 – hypertension, renal MeSH C12.777.419

June Sutor (1,198 words) [view diff] exact match in snippet view article find links to article

Hermon Dowling, R.; Rose, G. Alan; June Sutor, D. (29 May 1971). "Hyperoxaluria and Renal Calculi in Ileal Disease". The Lancet. Originally published

List of genetic disorders (969 words) [view diff] exact match in snippet view article find links to article

Hutchinson–Gilford progeria syndrome LMNA 1:18,000,000 Hyperlysinemia AASS recessive Hyperoxaluria, primary AGXT, GRHPR, DHDPSL Hyperphenylalaninemia 12q Hypoalphalipoproteinemia

Gluten-sensitive enteropathy–associated conditions (7,556 words) [view diff] exact match in snippet view article find links to article

PMID 17578801. S2CID 25201041. McDonald GB, Earnest DL, Admirand WH (1977). "Hyperoxaluria correlates with fat malabsorption in patients with sprue". Gut. 18 (7):

Crohn's disease (18,259 words) [view diff] exact match in snippet view article find links to article

due to calcium oxalate or uric acid stones. Calcium oxalate is due to hyperoxaluria typically associated with either distal ileal CD or ileal resection

Rainer Gruessner (1,263 words) [view diff] exact match in snippet view article find links to article

"Preemptive Liver Transplantation from a Living Related Donor for Primary Hyperoxaluria Type I". New England Journal of Medicine. 338 (26): 1924. doi:10

List of MeSH codes (C16) (6,496 words) [view diff] exact match in snippet view article

620 – glycogen storage disease type VIII MeSH C16.320.565.202.460 – hyperoxaluria, primary MeSH C16.320.565.202.589 – lactose intolerance MeSH C16.320

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

endosteal; 144750; LRP5 Hyperoxaluria, primary, type 1; 259900; AGXT Hyperoxaluria, primary, type II; 260000; GRHPR Hyperoxaluria, primary, type III; 613616;