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THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels

British journal of pharmacology, 2019-12, Vol.176 (S1), p.S142-S228

2019

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THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Overview

British journal of pharmacology, 2017-12, Vol.174 (S1), p.S1-S16

2017

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Relationship of Etiology to Treatment in Congenital Hypothyroidism

The journal of clinical endocrinology and metabolism, 2001-01, Vol.86 (1), p.186-191

2001

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Type 1 diabetes in Jewish Ethiopian immigrants in Israel: HLA class II immunogenetics and contribution of new environment

Human immunology, 2004-12, Vol.65 (12), p.1463-1468

2004

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Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism

Clinical endocrinology (Oxford), 2005-05, Vol.62 (5), p.547-553

2005

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Mechanism of corticotropin and cAMP induction of mitochondrial cytochrome P450 system enzymes in adrenal cortex cells

The Journal of biological chemistry, 1990-11, Vol.265 (33), p.20602-20608

1990

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An outbreak of echovirus 13 meningitis in central Israel

Epidemiology and infection, 2003-04, Vol.130 (2), p.257-262

2003

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Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

Nature genetics, 1996-03, Vol.12 (3), p.248-253

1996

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Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel

Pediatric diabetes, 2014-09, Vol.15 (6), p.422-427

2014

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Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects

The journal of clinical endocrinology and metabolism, 1991-11, Vol.73 (5), p.936-944

HANUKOGLU, A

1991

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Pulmonary Epithelial Sodium-Channel Dysfunction and Excess Airway Liquid in Pseudohypoaldosteronism

The New England journal of medicine, 1999-07, Vol.341 (3), p.156-162

1999

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Selective increases in adrenal steroidogenic capacity during acute respiratory disease in infants

European journal of endocrinology, 1995-11, Vol.133 (5), p.552-556

1995

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Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War

Pediatric diabetes, 2012-06, Vol.13 (4), p.326-333

2012

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Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish population

The Israel Medical Association journal, 2013-09, Vol.15 (9), p.477-480

2013

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Novel Mutations Responsible for Autosomal Recessive Multisystem Pseudohypoaldosteronism and Sequence Variants in Epithelial Sodium Channel α-, β-, and γ-Subunit Genes

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3344-3350

2002

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Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3341-3345

1995

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Extrapancreatic autoimmune manifestations in type 1 diabetes patients and their first-degree relatives: A multicenter study

Diabetes care, 2003-04, Vol.26 (4), p.1235-1240

2003

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The effect of endogenous dehydroepiandrosterone sulphate on antibody response to hepatitis B vaccine in neonates

The Israel Medical Association journal, 2000-03, Vol.2 (3), p.200-202

2000

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Cyclic Psychosis Associated with the Menstrual Cycle

British journal of psychiatry, 1993-12, Vol.163 (6), p.824-828

1993

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Severe pseudohypoaldosteronism in a pair of twins not associated with hydramnios

Pediatric nephrology (Berlin, West), 1996-08, Vol.10 (4), p.438-441

1996

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Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3341-3345

1995

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Amiloride-sensitive epithelial sodium channel subunits are expressed in human and mussel immunocytes

Developmental and comparative immunology, 2002-06, Vol.26 (5), p.395-402

2002

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Pseudohypoaldosteronism with increased sweat and saliva electrolyte values and frequent lower respiratory tract infections mimicking cystic fibrosis

The Journal of pediatrics, 1994-11, Vol.125 (5), p.752-755

1994

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Chronic urticaria in children: expanding the "autoimmune kaleidoscope"

Pediatrics (Evanston), 2000-11, Vol.106 (5), p.1139-1141

2000

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Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping

Human molecular genetics, 1996-02, Vol.5 (2), p.293-299

1996

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THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels

THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Overview

Relationship of Etiology to Treatment in Congenital Hypothyroidism

Type 1 diabetes in Jewish Ethiopian immigrants in Israel: HLA class II immunogenetics and contribution of new environment

Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism

Mechanism of corticotropin and cAMP induction of mitochondrial cytochrome P450 system enzymes in adrenal cortex cells

An outbreak of echovirus 13 meningitis in central Israel

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel

Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects

Pulmonary Epithelial Sodium-Channel Dysfunction and Excess Airway Liquid in Pseudohypoaldosteronism

Selective increases in adrenal steroidogenic capacity during acute respiratory disease in infants

Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War

Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish population

Novel Mutations Responsible for Autosomal Recessive Multisystem Pseudohypoaldosteronism and Sequence Variants in Epithelial Sodium Channel α-, β-, and γ-Subunit Genes

Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis

Extrapancreatic autoimmune manifestations in type 1 diabetes patients and their first-degree relatives: A multicenter study

The effect of endogenous dehydroepiandrosterone sulphate on antibody response to hepatitis B vaccine in neonates

Cyclic Psychosis Associated with the Menstrual Cycle

Severe pseudohypoaldosteronism in a pair of twins not associated with hydramnios

Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis

Amiloride-sensitive epithelial sodium channel subunits are expressed in human and mussel immunocytes

Pseudohypoaldosteronism with increased sweat and saliva electrolyte values and frequent lower respiratory tract infections mimicking cystic fibrosis

Chronic urticaria in children: expanding the "autoimmune kaleidoscope"

Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping

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