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Longer titles found: X-linked sideroblastic anemia and spinocerebellar ataxia (view)

searching for Sideroblastic anemia 16 found (55 total)

Metabolic myopathy (5,220 words) [view diff] no match in snippet view article find links to article

Metabolic myopathies are myopathies that result from defects in biochemical metabolism that primarily affect muscle. They are generally genetic defects

Zinc toxicity (996 words) [view diff] exact match in snippet view article find links to article

cause of sideroblastic anemia". West J Med. 152 (2): 190–192. PMC 1002314. PMID 2400417. Fiske, D.N. (1994). "Zinc-induced sideroblastic anemia: report

ALAS1 (1,075 words) [view diff] exact match in snippet view article find links to article

Cortesão E, Vidan J, Pereira J, et al. (2004). "Onset of X-linked sideroblastic anemia in the fourth decade". Haematologica. 89 (10): 1261–3. PMID 15477213

Mitochondrial myopathy (3,236 words) [view diff] exact match in snippet view article find links to article

"Phenotypic Series - PS600462 - Myopathy, lactic acidosis, and sideroblastic anemia (MLASA) - OMIM". www.omim.org. Retrieved 2023-11-30. "Allelic Variants

Red blood cell distribution width (772 words) [view diff] exact match in snippet view article find links to article

and microcytosis. 18% - 26% Moderate anisocytosis Severe iron deficiency anemia, megaloblastic anemia. > 26% Severe anisocytosis Sideroblastic anemia

Cotransporter (2,288 words) [view diff] exact match in snippet view article find links to article

SLC3A2 Lysinuric ABC-1, ABC1 Tangier disease ABC7, hABC7 X-linked sideroblastic anemia ABCR Stargardt disease, Fundus flavimaculatus AE1, SLC4A1 elliptocytosis

Tracey Rouault (620 words) [view diff] exact match in snippet view article find links to article

group helped to discover and characterize, including ISCU myopathy, sideroblastic anemia from GLRX5 deficiency, and lactic acidosis caused by mutations in

SUCLA2 (1,745 words) [view diff] exact match in snippet view article find links to article

synthetase and the heme-biosynthetic enzyme ALAS-E is disrupted in sideroblastic anemia". The Journal of Clinical Investigation. 105 (6): 757–64. doi:10

Mitochondrial ferritin (1,006 words) [view diff] exact match in snippet view article find links to article

"Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia". Blood. 101 (5): 1996–2000. doi:10.1182/blood-2002-07-2006. PMID 12406866

List of diseases (A) (1,929 words) [view diff] case mismatch in snippet view article

Diamond–Blackfan Anemia, hypoplastic, congenital Anemia, pernicious Anemia, sideroblastic Anemia sideroblastic spinocerebellar ataxia Anencephaly Anencephaly spina

Thiamine transporter 1 (1,882 words) [view diff] exact match in snippet view article find links to article

(February 2010). "Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations"

Copper deficiency (2,807 words) [view diff] exact match in snippet view article find links to article

an unusual pattern. This unusual pattern is also known as ringed sideroblastic anemia cells. The cause of neutropenia is still unclear; however, the arrest

RNA editing (7,435 words) [view diff] exact match in snippet view article find links to article

mutations in pseudouridine synthases cause mitochondrial myopathy, sideroblastic anemia (MLASA) and dyskeratosis congenital. Compared to the modifications

MERRF syndrome (1,929 words) [view diff] exact match in snippet view article find links to article

as episodes of nausea or vomiting. Multiple lipomas in the skin, sideroblastic anemia and pancytopenia in the metabolic system, or short stature might

List of diseases (M) (2,469 words) [view diff] exact match in snippet view article

areflexia Myopathy tubular aggregates Myopathy with lactic acidosis and sideroblastic anemia Myopathy with lysis of myofibrils Myopathy, centronuclear Myopathy

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

syndrome, hepatocerebral form; 251880; DGUOK Mitochondrial myopathy and sideroblastic anemia; 600462; PUS1 Mitochondrial neurogastrointestinal encephalomyopathy