Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Y Mitsuuchi
IDENTIFICATION OF a NEW MUTATION IN STEROID 11β-Hydroxylase DEFICIENCY
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Splicing Analysis of CYP11B1 Mutation in a Family Affected With 11β-Hydroxylase Deficiency: Case Report
BMC Endocrine Disorders
Medicine
Endocrinology
Metabolism
Diabetes
MINERAL OCORTICOID REPLACEMENT IN 11β-Hydroxylase DEFICIENCY (11-Ohd)
Pediatric Research
Child Health
Pediatrics
Perinatology
11β-Hydroxylase AND HYPERTENSION
Pediatric Research
Child Health
Pediatrics
Perinatology
Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency
Endocrinologia Japonica
The Combination of a Novel 2 Bp Deletion Mutation and p.D63H in CYP11B1 Cause Congenital Adrenal Hyperplasia Due to Steroid 11β-Hydroxylase Deficiency
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
The Non-Classical Form of Congenital Adrenal Cortical Hyperplasia Due to 11β-Hydroxylase Deficiency: The Description of Three Clinical Cases
Problemy Endokrinologii
Endocrinology
Metabolism
Diabetes
Mild Dopa-Responsive Dystonia in Heterozygous Tyrosine Hydroxylase Mutation Carrier: Evidence of Symptomatic Enzyme Deficiency?
Parkinsonism and Related Disorders
Gerontology
Geriatrics
Neurology
