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deficiency of monooxygenase

Known as: hydroxylase deficiency 
National Institutes of Health

Papers overview

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2014
2014
MLPA method in diagnostics of congenital adrenal hyperplasia caused by 21 hydroxylase deficiency
Nedostatak 21-hidroksilaze (21-OHD) najcesci je uzrok kongenitalne adrenalne hiperplazije (KAH), autosmno recesivnog poremecaja… 
2013
2013
A Rare Cause of Primary Amenorrhea and Hypokalemia; 17-A-Hydroxylase Deficiency (17OHD)
A 22-year-old female patient was admitted due to primary amenorrhea and chronic weakness. Parental consanguinity, delayed puberty… 
2012
2012
Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH - 21OHD).
2010
2010
A case of dopamine beta hydroxylase deficiency, a limited adrenergic neuropathy: treatment with L-DOPS
2007
2007
Adrenal rest tissue in gonads in 70 French patients with classical congenital adrenal hyperplasia (21 hydroxylase deficiency)
2001
2001
21 hydroxylase deficiency
1994
1994
Molecular defects of Chinese patients with 21 hydroxylase deficiency
1982
1982
[Genetic of the 21 hydroxylase deficiency].
A dose genetic linkage exist between the HLA complex (especially HLA-B), and the 21 hydroxylase deficiency form of adrenal… 
1981
1981
Defective 11 beta hydroxylation in patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency.
1974
1974
[Plasmatic 17-alpha-hydroxyprogesterone in congenital adrenal hyperplasia due to 21 hydroxylase deficiency, treated and untreated].