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Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings

Metabolic brain disease, 2024-06, Vol.39 (5), p.909-913

2024

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Diagnostic challenges and outcome of fatty acid oxidation defects in a tertiary care center in Lebanon

Orphanet journal of rare diseases, 2024-08, Vol.19 (1), p.315-9, Article 315

2024

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Higher Incidence Rates of Hypothyroidism and Late TSH Rise in Preterm Very-Low-Birth-Weight Infants at a Tertiary Care Center

Hormone research in paediatrics, 2018-01, Vol.89 (4), p.224-232

2018

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Diagnosis and management of symptomatic profound biotinidase deficiency in a tertiary care center in Lebanon

Clinical biochemistry, 2020-12, Vol.86, p.52-55

2020

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25-Hydroxyvitamin D Assay Variations and Impact on Clinical Decision Making

The journal of clinical endocrinology and metabolism, 2012-03, Vol.97 (3), p.835-843

2012

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Outcome of Nonketotic Hyperglycinemia in Lebanon: 14-Year Retrospective Review

Neuropediatrics, 2019-08, Vol.50 (4), p.235-243

2019

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CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population

Annals of human genetics, 2022-03, Vol.86 (2), p.80-86

2022

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Limitations of platform assays to measure serum 25OHD level impact on guidelines and practice decision making

Metabolism, clinical and experimental, 2018-12, Vol.89, p.1-7

2018

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

Clinical biochemistry, 2013-12, Vol.46 (18), p.1787-1792

2013

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Extended Use of Serum Free Light Chain as a Biomarker in Lymphoproliferative Disorders: A Comprehensive Review

American journal of clinical pathology, 2012-06, Vol.137 (6), p.890-897

2012

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Taurine Intestinal Absorption and Renal Excretion Test in Diabetic Patients: A pilot study

Diabetes care, 2007-10, Vol.30 (10), p.2652-2654

2007

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Dietary Zinc Intake and Plasma Zinc Concentrations in Children with Short Stature and Failure to Thrive

Annals of nutrition and metabolism, 2016-01, Vol.69 (1), p.9-14

2016

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Correlation of methylenetetrahydrofolate reductase polymorphisms with homocysteine metabolism in healthy Lebanese adults

Gene, 2012-08, Vol.504 (2), p.175-180

2012

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Experience With Hyperphenylalaninemia in a Developing Country: Unusual Clinical Manifestations and a Novel Gene Mutation

Journal of child neurology, 2011-02, Vol.26 (2), p.142-146

2011

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Relation Between Iron-Overload Indices, Cardiac Echo-Doppler, and Biochemical Markers in Thalassemia Intermedia

The American journal of cardiology, 2008-08, Vol.102 (3), p.363-367

2008

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Taurine Intestinal Absorption and Renal Excretion Test in Diabetic Patients

Diabetes care, 2007-10, Vol.30 (10), p.2652-2654

2007

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Trace metals (lead and cadmium exposure screening)

Analytical chemistry (Washington), 1995-06, Vol.67 (12), p.405-410

Daher, Rose T

1995

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The use of a reverse hybridization strip assay for the study of hemochromatosis-associated gene mutations in Lebanon

Genetic testing and molecular biomarkers, 2011-12, Vol.15 (12), p.909-911

2011

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Should we screen for hereditary hemochromatosis in healthy Lebanese: a pilot study

Molecular biology reports, 2012, Vol.39 (1), p.753-759

2012

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12410 Intra-operative Parathyroid Hormone Monitoring: Comparative Evaluation Of Sampling Sites And Assay Methods

Journal of the Endocrine Society, 2024-10, Vol.8 (Supplement_1)

2024

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Patterns of monoclonal components and their correlation with different analytical parameters

Saudi medical journal, 2011-03, Vol.32 (3), p.308

2011

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ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature

Molecular biology reports, 2007-12, Vol.34 (4), p.267-270

2007

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Effect of vitamin D replacement on indexes of insulin resistance in overweight elderly individuals: a randomized controlled trial12

The American journal of clinical nutrition, 2016-08, Vol.104 (2), p.315-323

2016

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Incidence of Alpha-Globin Gene Defect in the Lebanese Population: A Pilot Study

BioMed research international, 2015-01, Vol.2015 (2015), p.1-3

2015

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High prevalence of MTHFR gene A1298C polymorphism in Lebanon

Genetic testing, 2008-03, Vol.12 (1), p.75-80

2008

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Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings

Diagnostic challenges and outcome of fatty acid oxidation defects in a tertiary care center in Lebanon

Higher Incidence Rates of Hypothyroidism and Late TSH Rise in Preterm Very-Low-Birth-Weight Infants at a Tertiary Care Center

Diagnosis and management of symptomatic profound biotinidase deficiency in a tertiary care center in Lebanon

25-Hydroxyvitamin D Assay Variations and Impact on Clinical Decision Making

Outcome of Nonketotic Hyperglycinemia in Lebanon: 14-Year Retrospective Review

CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population

Limitations of platform assays to measure serum 25OHD level impact on guidelines and practice decision making

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

Extended Use of Serum Free Light Chain as a Biomarker in Lymphoproliferative Disorders: A Comprehensive Review

Taurine Intestinal Absorption and Renal Excretion Test in Diabetic Patients: A pilot study

Dietary Zinc Intake and Plasma Zinc Concentrations in Children with Short Stature and Failure to Thrive

Correlation of methylenetetrahydrofolate reductase polymorphisms with homocysteine metabolism in healthy Lebanese adults

Experience With Hyperphenylalaninemia in a Developing Country: Unusual Clinical Manifestations and a Novel Gene Mutation

Relation Between Iron-Overload Indices, Cardiac Echo-Doppler, and Biochemical Markers in Thalassemia Intermedia

Taurine Intestinal Absorption and Renal Excretion Test in Diabetic Patients

Trace metals (lead and cadmium exposure screening)

The use of a reverse hybridization strip assay for the study of hemochromatosis-associated gene mutations in Lebanon

Should we screen for hereditary hemochromatosis in healthy Lebanese: a pilot study

12410 Intra-operative Parathyroid Hormone Monitoring: Comparative Evaluation Of Sampling Sites And Assay Methods

Patterns of monoclonal components and their correlation with different analytical parameters

ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature

Effect of vitamin D replacement on indexes of insulin resistance in overweight elderly individuals: a randomized controlled trial12

Incidence of Alpha-Globin Gene Defect in the Lebanese Population: A Pilot Study

High prevalence of MTHFR gene A1298C polymorphism in Lebanon

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