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Publications by M Roubiceck
Familial Neurohypophyseal Diabetes Insipidus (Nhdi) Due to a Mutation in the Vasopressin-Neurophysine Ii (Vp-NPH Ii) Gene
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Novel Mutant Vasopressin-Neurophysin II Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Vasopressin Function in Familial Cranial Diabetes Insipidus.
Postgraduate Medical Journal
Medicine
A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant With Nephrogenic Diabetes Insipidus
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Continuous Vasopressin Replacement in Diabetes Insipidus.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Mutant Vasopressin Precursors That Cause Autosomal Dominant Neurohypophyseal Diabetes Insipidus Retain Dimerization and Impair the Secretion of Wild-Type Proteins
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
V2 Vasopressin Receptor Mutation Y205c Causing Nephrogenic Diabetes Insipidus Retains Partial Function in Vitro. † 885
Pediatric Research
Child Health
Pediatrics
Perinatology
Nephrogenic Diabetes Insipidus Due to Urinary Tract Obstruction: A Systematic Review
Internal Medicine and Medical Investigation Journal
Familial Partial Lipodystrophy Type 3 Due to PPARgamma Mutation: Presentation With Diabetes and Severe Hypertriglyceridemia
Endocrine Abstracts
Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2Receptor Mutant by Cell-Penetrating Peptides
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
