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searching for Fanconi syndrome 12 found (79 total)

Wissler's syndrome (178 words) [view diff] exact match in snippet view article find links to article

Wissler's syndrome Other names Wissler's disease or Wissler-Fanconi syndrome Specialty Immunology, rheumatology

Multidrug resistance-associated protein 2 (1,709 words) [view diff] exact match in snippet view article find links to article

anions inhibit mitochondrial DNA synthesis, it may cause iatrogenic Fanconi syndrome. The nucleoside phosphonate adefovir is a MRP2 inhibitor that has been

Fanconi–Bickel syndrome (257 words) [view diff] no match in snippet view article find links to article

Fanconi–Bickel syndrome is a form of glycogen storage disease named for Guido Fanconi and Horst Bickel, who first described it in 1949. It is associated

GRACILE syndrome (609 words) [view diff] exact match in snippet view article find links to article

serum ferritin Intrauterine growth retardation Lactic acidosis Renal Fanconi syndrome Other symptoms that happen in a smaller percentage of people with GRACILE

Genevieve Stearns (694 words) [view diff] case mismatch in snippet view article find links to article

D.; Stearns, Genevieve (1941-05-01). "Late Rickets Resembling the Fanconi Syndrome". Archives of Pediatrics & Adolescent Medicine. 61 (5): 1012. doi:10

Proximal tubule (1,519 words) [view diff] exact match in snippet view article find links to article

from gram-negative bacteria). Renal tubular acidosis (proximal type) (Fanconi syndrome) occurs when the PTECs are unable to properly reabsorb glomerular filtrate

Fumarylacetoacetate hydrolase (2,536 words) [view diff] exact match in snippet view article find links to article

tubular injury, hepatic necrosis, episodic weakness, seizures. Renal Fanconi syndrome and Porphyric crises are also cited in addition to liver and renal

Cystatin C (6,278 words) [view diff] exact match in snippet view article find links to article

"Glomerular protein sieving and implications for renal failure in Fanconi syndrome". Kidney International. 60 (5): 1885–92. doi:10.1046/j.1523-1755.2001

Prader–Willi syndrome (3,964 words) [view diff] exact match in snippet view article find links to article

Prader–Willi syndrome Other names Prader–Labhart–Willi-Fanconi syndrome Prader-Willi-Down syndrome 15-year-old patient with PWS Pronunciation /ˈprɑːdər

Osteitis fibrosa cystica (4,028 words) [view diff] exact match in snippet view article find links to article

susceptible to ill effects from fluoride exposure which manifest in bones. Fanconi syndrome: decrease amino acids, phosphate, glucose, bicarbonate and potassium

Oliver Wrong (2,198 words) [view diff] case mismatch in snippet view article find links to article

his co-workers Norden and Feest reported it as a form of the renal 'Fanconi Syndrome'. A very similar hereditary clinical syndrome was reported by Scheinman

List of lay Catholic scientists (4,579 words) [view diff] exact match in snippet view article find links to article

biochemist who defined new amino-acid diseases such as various forms of Fanconi syndrome, Hartnup disease, argininosuccinic aciduria and homocystinuria César-Mansuète