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Adel Gassab Mohammed on Muck Rack

Adel Gassab Mohammed

As seen in: Nature, Dialnet - Universidad de La Rioja, JAAD Case Reports
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Articles

Steroid formulation, standardized prednisolone-equivalent dose, and thyroid–adrenal axis function in 28,695 adults: a real-world cross-sectional study

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By Adel Gassab Mohammed, Abbas Mansour, Rudha Naser Hussein
| Nature Verified
Abstract Exogenous steroid misuse is an increasingly recognized public health concern with potential consequences for hypothalamic–pituitary–thyroid (HPT) axis regulation. However, dose-standardized evidence linking specific steroid formulations to thyroid function markers remains scarce. To examine associations between steroid type and prednisolone-equivalent dose with thyroid function markers (TSH and FT4) and adrenal axis markers in a large adult clinical cohort.
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The Impact of Tax Legislation on Public Shareholding Companies Tax Disclosure: A Comparative Study Between the Jordanian Tax System and the U.S. Tax System (State of Illinois)

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By Khalid Amayreh, Adel Gassab Mohammed, Adel Mohammed Qatawneh, Ayman Bader
| Dialnet - Universidad de La Rioja
The Impact of Tax Legislation on Public Shareholding Companies Tax Disclosure: A Comparative Study Between the Jordanian Tax System and the U.S. Tax System (State of Illinois) Autores: Adel Mohammed Qatawneh, Ayman Bader, Khalid Thaher Amayreh Localización: International Journal of Professional Business Review: Int. J. Prof.Bus. Rev., ISSN 2525-3654, ISSN-e 2525-3654, Vol. 8, Nº.
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H syndrome with low bone mineral density associated with hypovitaminosis D and low insulin-like growth factor 1

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By Khalil I. Al-Hamdi, Dooha Khaleel Ismael, Adel Gassab Mohammed, Ussama M. Makki
| JAAD Case Reports Verified
Key words genetic genodermatosis H syndrome hallux valgus SLC29A3 hyperpigmentation hypertrichosis Abbreviation used: BMD (bone mineral density), DXA (dual-energy x-ray absorptiometry) Introduction H syndrome is a rare autosomal recessive disorder that occurs because of mutations in the SLC29A3 gene, encoding the human equilibrative nucleoside transporter, which is a protein located in endosomes, lysosomes, and mitochondria. , 2 Bloom J.L. Lin C. Imundo L. et al.
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