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Diabetes insipidus: Differential diagnosis and management

Baillière's best practice & research. Clinical endocrinology & metabolism, 2016-03, Vol.30 (2), p.205-218

Robertson, Gary L., MD

2016

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Recent Studies of Exotic Hadrons at the LHCb Experiment

SciPost physics proceedings, 2022-07 (8), p.030, Article 030

Robertson, Gary

2022

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Copeptin in the Diagnosis of Diabetes Insipidus

The New England journal of medicine, 2018-11, Vol.379 (18), p.1784

Robertson, Gary L

2018

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Familial forms of diabetes insipidus: clinical and molecular characteristics

Nature reviews. Endocrinology, 2011-12, Vol.7 (12), p.701-714

2011

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Regulation of Arginine Vasopressin in the Syndrome of Inappropriate Antidiuresis

The American journal of medicine, 2006-07, Vol.119 (7), p.S36-S42

Robertson, Gary L.

2006

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Vaptans for the treatment of hyponatremia

Nature reviews. Endocrinology, 2011-03, Vol.7 (3), p.151-161

Robertson, Gary L

2011

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Treatment of Neurohypophyseal Diabetes Insipidus

The journal of clinical endocrinology and metabolism, 2013-10, Vol.98 (10), p.3958-3967

2013

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A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner

The journal of clinical endocrinology and metabolism, 2022-05, Vol.107 (6), p.e2513-e2522

2022

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Temporal delays and individual variation in antidiuretic response to desmopressin

American journal of physiology. Renal physiology, 2013-02, Vol.304 (3), p.F268-F278

2013

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Copeptin in the Diagnosis of Diabetes Insipidus

The New England journal of medicine, 2018-11, Vol.379 (18), p.1784-1786

2018

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The effects of mutating Tyr9 and Arg15 on the structure, stability, conformational dynamics and mechanism of GSTA3-3

Biophysical chemistry, 2017-05, Vol.224, p.40-48

2017

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Author Correction: Optimized model architectures for deep learning on genomic data

Communications biology, 2024-05, Vol.7 (1), p.625-625, Article 625

2024

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Optimized model architectures for deep learning on genomic data

Communications biology, 2024-04, Vol.7 (1), p.516-516, Article 516

2024

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Exposures of preschool children to chlorpyrifos and its degradation product 3,5,6-trichloro-2-pyridinol in their everyday environments

Journal of exposure analysis and environmental epidemiology, 2005-07, Vol.15 (4), p.297-309

2005

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Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene

Clinical endocrinology (Oxford), 2008-03, Vol.68 (3), p.395-403

2008

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Hypernatremic Hydrophobic Transient Adipsia Without Organic or Severe Psychiatric Disorder

The journal of clinical endocrinology and metabolism, 2019-11, Vol.104 (11), p.5427-5430

2019

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Response to Letter to the Editor: “Hypernatremic Hydrophobic Transient Adipsia without Organic or Severe Psychiatric Disorder”

The journal of clinical endocrinology and metabolism, 2020-03, Vol.105 (3), p.e906-e906

2020

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Semivolatile Organic Compounds in Residential Air along the Arizona−Mexico Border

Environmental science & technology, 2009-05, Vol.43 (9), p.3054-3060

2009

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Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus

Journal of the American Society of Nephrology, 2000-06, Vol.11 (6), p.1044-1054

2000

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Differential Cellular Handling of Defective Arginine Vasopressin (AVP) Prohormones in Cells Expressing Mutations of the AVP Gene Associated with Autosomal Dominant and Recessive Familial Neurohypophyseal Diabetes Insipidus

The journal of clinical endocrinology and metabolism, 2004-09, Vol.89 (9), p.4521-4531

2004

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Autosomal Dominant Neurohypophyseal Diabetes Insipidus due to Substitution of Histidine for Tyrosine2 in the Vasopressin Moiety of the Hormone Precursor

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3351-3355

2002

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Expression of three different mutations in the arginine vasopressin gene suggests genotype-phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds

Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.207-216

2005

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Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis

European journal of human genetics : EJHG, 2004-01, Vol.12 (1), p.44-51

2004

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Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes

Molecular endocrinology (Baltimore, Md.), 1997-11, Vol.11 (12), p.1806-1813

1997

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Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

Clinical endocrinology (Oxford), 2004-01, Vol.60 (1), p.125-136

2004

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Diabetes insipidus: Differential diagnosis and management

Recent Studies of Exotic Hadrons at the LHCb Experiment

Copeptin in the Diagnosis of Diabetes Insipidus

Familial forms of diabetes insipidus: clinical and molecular characteristics

Regulation of Arginine Vasopressin in the Syndrome of Inappropriate Antidiuresis

Vaptans for the treatment of hyponatremia

Treatment of Neurohypophyseal Diabetes Insipidus

A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner

Temporal delays and individual variation in antidiuretic response to desmopressin

Copeptin in the Diagnosis of Diabetes Insipidus

The effects of mutating Tyr9 and Arg15 on the structure, stability, conformational dynamics and mechanism of GSTA3-3

Author Correction: Optimized model architectures for deep learning on genomic data

Optimized model architectures for deep learning on genomic data

Exposures of preschool children to chlorpyrifos and its degradation product 3,5,6-trichloro-2-pyridinol in their everyday environments

Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene

Hypernatremic Hydrophobic Transient Adipsia Without Organic or Severe Psychiatric Disorder

Response to Letter to the Editor: “Hypernatremic Hydrophobic Transient Adipsia without Organic or Severe Psychiatric Disorder”

Semivolatile Organic Compounds in Residential Air along the Arizona−Mexico Border

Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus

Differential Cellular Handling of Defective Arginine Vasopressin (AVP) Prohormones in Cells Expressing Mutations of the AVP Gene Associated with Autosomal Dominant and Recessive Familial Neurohypophyseal Diabetes Insipidus

Autosomal Dominant Neurohypophyseal Diabetes Insipidus due to Substitution of Histidine for Tyrosine2 in the Vasopressin Moiety of the Hormone Precursor

Expression of three different mutations in the arginine vasopressin gene suggests genotype-phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds

Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis

Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes

Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

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