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Hypomagnesemia 1, Intestinal

Known as: Hypomagnesemia with Secondary Hypocalcemia, HSH, HOMG 
National Institutes of Health

Related topics

Related topics

8 relations
Autosomal recessive inheritanceSeizuresSpasmTRPM6, 1-BP DEL, 1280A

Broader (2)

HypocalcemiaMagnesium Deficiency

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
HIV Rapid Testing Programs in Non-Clinical Settings have the Potential to Constitute a Major Diagnostic Option for MSM in Spain
We analyze the impact of HIV rapid testing (RT) programs in non-clinical settings (NCS) by evaluating their contribution to new… 
2015
2015
Hypomagnesemia due to two novel TRPM6 mutations
Abstract Background: Although most hypocalcemia with hypomagenesemia in the neonatal period is due to transient neonatal… 
2012
2012
Surface shear rheology of hydrophobin adsorption layers: laws of viscoelastic behaviour with applications to long-term foam stability.
The long-term stabilization of foams by proteins for food applications is related to the ability of proteins to form dense and… 
2011
2011
Evaluation of accuracy of Euroscore risk model in prediction of perioperative mortality after coronary bypass graft surgery in Isfahan*
BACKGROUND: This study aimed to evaluate the accuracy of Euroscore (European System for Cardiac Operative Risk Evaluation) in… 
2008
2008
A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation
An offspring of marriage between two first cousins presented with atonic seizures developed on the 20th day of life. The physical… 
2007
2007
Diagnóstico de la infección por Chlamydia trachomatis en un centro de diagnóstico y prevención de infecciones de transmisión sexual: evaluación de los exudados cervicales, uretrales y rectales…
Introduccion Se analizaron las caracteristicas clinicas y epidemiologicas de la infeccion por Chlamydia trachomatis en pacientes… 
2006
2006
Genetic background of HSH in three Polish families and a patient with an X;9 translocation
Hypomagnesemia with secondary hypocalcemia (HSH) is a rare inherited disease, characterised by neurological symptoms, such as… 
1995
1995
Thrombolysis with recombinant unglycosylated single-chain urokinase-type plasminogen activator (saruplase) in acute myocardial infarction: influence of heparin on early patency rate (LIMITS study…
1994
1994
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.
Magnesium-dependent hypocalcaemia (HSH), a rare inherited disease, is caused by selective disorders of magnesium absorption. Both… 
1990
1990
Metabolic Response to Oral Challenge of Hydrogenated Starch Hydrolysate Versus Glucose In Diabetes
Our objective was to determine whether 1) hydrogenated starch hydrolysates (HSHs), bulking/sweetening agents used in hard candies… 
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