DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Bartter syndrome
Bartter syndrome
Congenital Chloride Diarrhea in a Bartter Syndrome Misdiagnosed
Pseudo-Bartter Syndrome As the Initial Presentation of Cystic Fibrosis in Infants: a Paediatrics Section Paediatrics Series of Three Cases and Review of Literature
Hypokalemic Periodic Paralysis - an Owner's Manual
Inherited Renal Tubulopathies—Challenges and Controversies
Pdf
The Role of Potassium Recirculation in Cochlear Amplification
Date: 1/9/2017 Question: Botulism Is an Uncommon Disorder Caused By
Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery
A Man with a Worrying Potassium Deficiency
Liddle's Syndrome
Pseudohypoaldosteronism Due to Sweat Gland Dysfunction
Antenatal Bartter Syndrome Resembling Nephrogenic Diabetes Insipidus in a 5-Year-Old Boy Gwo-Tsann Chuang A, Shih-Hua Lin B, Yong-Kwei Tsau A, I-Jung Tsai A,*
Blueprint Genetics Bartter Syndrome Panel
Pseudo-Bartter's Syndrome in Patients with Cystic
Bartter's Syndrome
Heavy Metal Burden Presenting As Bartter Syndrome Walter J
Gitelman's Syndrome with Silent Thyroiditis
The Channelopathies: Novel Insights Into Molecular and Genetic Mechanisms of Human Disease
Top View
Recurrent Hypokalemic Periodic Paralysis Unmasks Sjogren
Bartter Syndrome
Pseudo-Bartter's Syndrome in Cystic Fibrosis
Hypokalemic Periodic Paralysis with Arrhythmia a Case Report and Review of Literature
Approach to Renal Tubular Disorders
A Genetic Investigation of the Muscle and Neuronal Channelopathies: from Sanger to Next – Generation Sequencing
Chloride Channel Diseases Resulting from Impaired Transepithelial Transport Or Vesicular Function
Pseudo-Bartter's Syndrome in Patients with Cystic Fibrosis
Clinical Application of a Phenotype-Based NGS Panel for Differential Diagnosis of Inherited Kidney Disease and the Beyond
Tubulointerstitial Disease
SKELETAL MUSCLE CHANNELOPATHIES Mus7 (1)
Case Report Bartter Syndrome Type 1 Presenting As Nephrogenic Diabetes Insipidus
Cystic Fibrosis in an Infant: Presented As Pseudo Bartter Syndrome
Chondrocalcinosis and Osteoporosis in a Patient with Renal Tubular Disorder
Connexin 30 Deficiency Impairs Renal Tubular ATP Release and Pressure Natriuresis
Pseudo-Bartter As an Initial Presentation of Cystic Fibrosis. a Case Report and Review of the Literature M.A
Expanded Genetic Screening Panel for the Ashkenazi Jewish Population
500 PLUS Panel Understanding More Means Empowering More Your Patients Are Asking for Even More Insight As They Plan for the Future
Bartter Syndrome: Causes, Diagnosis, and Treatment
Nephrocalcinosis: a Review of Monogenic Causes and Insights They Provide Into This Heterogeneous Condition
Ion Channelopathies in Endocrinology
Dent Disease Is an Underrecognized Cause of Focal Glomerulosclerosis
Paralysis After Treatment for Thyrotoxicosis Postgrad Med J: First Published As 10.1136/Pgmj.73.861.445 on 1 July 1997
Antenatal Bartter Syndrome Resembling
Channelopathies: a Link Between Brain and Heart: the Model of Epilepsy
Pseudo ‑Bartter Syndrome As an Initial Presentation of Cystic Fibrosis
Bartter Syndrome, Gitelman Syndrome and Homoeopathy
Society of General Internal Medicine
377 Part 4—Schedule for Rating Disabilities
Jemds.Com Case Report
Ease with Gitelman Syndrome: GS Is a Rare Autosomal Recessive Disorder Which Is Caused by Mutations in the SLC12A3 Gene
Diagnosis and Management of Bartter Syndrome: Consensus and Recommendations from the Erknet Working Group for Tubular Disorders
Cystic Fibrosis Presenting As Pseudo-Bartter Syndrome: an Important Diagnosis That Is Missed!
Muscle Disease in Medical and Systemic Disorder
Thyrotoxic Hypokalemic Periodic Paralysis a Neuroendocrine Emergency: Review Article
Ion Channel Diseases
A Practical Approach to Refractory Hypokalaemia: a Rare Presentation
Bartter/Gitelman Syndrome Based on Clinical Characteristics
Complicated Gitelman Syndrome and Autoimmune Thyroid Disease
Case Report: Recurrent Hypokalemic Periodic Paralysis Associated With
Esit Diagnosis List
Bartter Syndrome with Nephrogenic Diabetes Insipidus and Vitamin D
Salt-Losing Tubulopathies in Children: What’S New, What’S Controversial?