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Homocystinuria
LE WE PMID CA
Homocystinuria6781Homozystinurie

Amino acids (Hereditary diseases)

Amino acids (Sulfur containing)

CNS (Stroke BASKET)

Cystathionine beta synthase

Homocysteine

Homocystinuria

Methionine metabolic cycle

Transsulfuration

Urea cycle

1971  
1
Homocystinuria. Review of four cases.
[5579166] Br J Ophthalmol 55(5): 338-42 (1971)
2003  
2
Hyperhomocysteinemia--case report.
[12769002] Rev Port Cardiol 22(2): 223-30 (2003)
2006  
3
Inborn errors of sulfur-containing amino acid metabolism.
[16702350] J Nutr 136(6 Suppl): 1750S-1754S (2006)
2010  
4
Inherited metabolic disorders and stroke part 2: homocystinuria, organic acidurias, and urea cycle disorders.
[20142522] Arch Neurol 67(2): 148-53 (2010)
2010  
5
A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiency.
[19819175] Mol Genet Metab 99(1): 1-3 (2010)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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