Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 7 of 7 entries
Sorted by: Best Match Show Resources per page
Incontinentia pigmenti.

Annals of Saudi medicine

Al-Khenaizan S.
PMID: 17264639
Ann Saudi Med. 2000 Sep-Nov;20(5):424-6. doi: 10.5144/0256-4947.2000.424.

No abstract available.

Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations.

Therapeutics and clinical risk management

Nashabat M, Al-Khenaizan S, Alfadhel M.
PMID: 29440907
Ther Clin Risk Manag. 2018 Feb 02;14:225-229. doi: 10.2147/TCRM.S151732. eCollection 2018.

Methionine adenosyltransferase (MAT) I/III deficiency (OMIM # 250850) is caused by a mutation in

Topical timolol for vasculitis ulcer: A potential healing approach.

JAAD case reports

Alsaad AMS, Alsaad SM, Fathaddin A, Al-Khenaizan S.
PMID: 31508472
JAAD Case Rep. 2019 Aug 30;5(9):812-814. doi: 10.1016/j.jdcr.2019.07.016. eCollection 2019 Sep.

No abstract available.

Patients, Prescribers, and Institutional Factors Associated with Inappropriate Use of Acid Suppressive Therapy in Medical Wards: An Experience of a Single-Center in Saudi Arabia.

International journal of general medicine

Korayem GB, Alkanhal R, Almass R, Alkhunaizan S, Alharthi G, Bin Sheraim N, Alqahtani S, Alkofide H.
PMID: 34511990
Int J Gen Med. 2021 Aug 30;14:5079-5089. doi: 10.2147/IJGM.S328914. eCollection 2021.

PURPOSE: To identify factors associated with inappropriate acid-suppressive therapy (AST) use in hospitalized medical ward patients.PATIENTS AND METHODS: This was a combined retrospective cohort study reviewing the electronic medical records of medical ward in a secondary university hospital between...

Propranolol-induced hyperkalemia in the management of infantile hemangioma.

JAAD case reports

Al-Rwebah H, Alkhodair R, Al-Khenaizan S.
PMID: 32258322
JAAD Case Rep. 2020 Mar 25;6(4):359-361. doi: 10.1016/j.jdcr.2020.01.028. eCollection 2020 Apr.

No abstract available.

Ichthyosis Prematurity Syndrome: A Rare Form but Easily Recognizable Ichthyosis.

Case reports in dermatology

Al-Khenaizan S, AlSwailem A, AlBalwi MA.
PMID: 34720920
Case Rep Dermatol. 2021 Sep 21;13(3):470-473. doi: 10.1159/000519035. eCollection 2021.

Ichthyosis prematurity syndrome is a rare autosomal recessive genodermatosis that is associated with mutations in the

Implantation of a cardiac pacemaker to circumvent complete heart block in a life-threatening hemangioma to allow the use of propranolol.

JAAD case reports

Al-Khenaizan S, Faqeeh H.
PMID: 31646159
JAAD Case Rep. 2019 Sep 24;5(10):844-845. doi: 10.1016/j.jdcr.2019.06.029. eCollection 2019 Oct.

No abstract available.

Showing 1 to 7 of 7 entries