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Publications by M. Zaidi
Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Osteoclastic Inhibition: An Action of Nitric Oxide Not Mediated by Cyclic GMP.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Human Genetics
Genetics
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia
Pediatric Research
Child Health
Pediatrics
Perinatology
Long-Term Glucocorticoid Effect on Bone Mineral Density in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy
Balkan Journal of Medical Genetics
Genetics
