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Publications by G. L. Robertson

Vasopressin Function in Familial Cranial Diabetes Insipidus.

Postgraduate Medical Journal

English

Related publications

Novel Mutant Vasopressin-Neurophysin II Gene Associated With Familial Neurohypophyseal Diabetes Insipidus

Endocrine Journal

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Continuous Vasopressin Replacement in Diabetes Insipidus.

Archives of Disease in Childhood

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V2 Vasopressin Receptor Mutation Y205c Causing Nephrogenic Diabetes Insipidus Retains Partial Function in Vitro. † 885

Pediatric Research

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Cranial Diabetes Insipidus Caused by Giant Cell Arteritis.

Postgraduate Medical Journal

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Familial Neurohypophyseal Diabetes Insipidus (Nhdi) Due to a Mutation in the Vasopressin-Neurophysine Ii (Vp-NPH Ii) Gene

Pediatric Research

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Safety of Prescribing for Inpatients With Cranial Diabetes Insipidus (CDI): A Southwest Peninsula Audit

Endocrine Abstracts

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Diabetes Insipidus

Pediatrics in Review

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Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2Receptor Mutant by Cell-Penetrating Peptides

Journal of Biological Chemistry

Molecular Biology

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Experimental Diabetes Insipidus

English