Lista de obras - Mohammad Zouheir Habbal - Dominio Público Uruguay

A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype

artículo científico publicado en 2006

A novel genotype c.1228C>G/c.1448C-1498C (L371V/Rec-NciI) in a 3-year-old child with type 1 Gaucher disease

scientific article published on 01 January 2008

Bacterial contamination positively interferes with beta-glucosidase and hexosaminidase assays in white blood cell lysates

artículo científico publicado en 2008

Comparative pharmacokinetics and metabolic pathway of gemcitabine during intravenous and intra-arterial delivery in unresectable pancreatic cancer patients.

artículo científico publicado en 2005

Cysteamine-induced duodenal ulcer: effects on calcium absorption across rat duodenum

artículo científico publicado en 1987

Cytoskeletal control of calcium absorption across the rat small intestine.

artículo científico publicado en 1988

Determination of the gamma G/gamma A ratio in homozygous beta-thalassemic patients among a Lebanese population

scientific article published on 01 December 1984

Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience.

artículo científico publicado en 2013

Dopamine receptors in normal and diabetic liver plasma membrane.

artículo científico publicado en 1986

Effect of enzymatic digestion on phenylalanine transport across the small intestine.

artículo científico publicado en 1986

Enzymatic inhibition of lysine transport across the small intestine in vivo

scientific article published on 01 January 1988

First report of a deletion encompassing an entire exon in the homogentisate 1,2-dioxygenase gene causing alkaptonuria.

artículo científico publicado en 2014

Gaucher disease: different clinical manifestations associated with a rare mutation (R48W) in a Lebanese family.

artículo científico publicado en 2007

High protein vs high carbohydrate hypoenergetic diet for the treatment of obese hyperinsulinemic subjects

artículo científico publicado en 1999

Influence of CYP2C9 and VKORC1 polymorphisms on warfarin and acenocoumarol in a sample of Lebanese people.

artículo científico publicado en 2010

Mevalonate metabolism in supernatant fractions of lysates of Lactobacillus plantarum.

artículo científico publicado en 1970

Novel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardation

artículo científico publicado en 2006

Novel mutation, L371V, causing multigenerational Gaucher disease in a Lebanese family.

artículo científico publicado en 2004

Obesity is associated with insulin resistance and components of the metabolic syndrome in Lebanese adolescents.

artículo científico publicado en 2012

Prostacyclin-enhanced calcium sequestration by microsomes isolated from rat left ventricle

scientific article published on 01 June 1988

Prostacyclin-inhibition of lysine accumulation by the rat left ventricle