Mohammed Alpakra

Khamis Mushait, Saudi Arabia

Last Updated: 09/26/2026

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Found 9 publications

A Digital Patient Engagement and Monitoring System to Improve Quality, Safety, and Continuity of Care for Pediatric Sickle Cell Anemia: A Cross-Sectional Study of Caregiver Perceptions.

A Digital Patient Engagement and Monitoring System to Improve Quality, Safety, and Continuity of Care for Pediatric Sickle Cell Anemia: A Cross-Sectional Study of Caregiver Perceptions.

Journal: Cureus
Published: January 15, 2026

The Correlation Between Vitamin D Deficiency and Anemia: A Systematic Review.

The Correlation Between Vitamin D Deficiency and Anemia: A Systematic Review.

Journal: Cureus
Published: August 05, 2025

Congenital Mesoblastic Nephroma Mixed Subtype: A Case Report of a Rare Neonatal Tumor.

Congenital Mesoblastic Nephroma Mixed Subtype: A Case Report of a Rare Neonatal Tumor.

Journal: Cureus
Published: October 02, 2024

The Association Between Sickle Cell Anemia and Cognitive Dysfunction: A Systematic Review.

The Association Between Sickle Cell Anemia and Cognitive Dysfunction: A Systematic Review.

Journal: Cureus
Published: September 10, 2024

A Novel Variant in the DIAPH1 Gene Causing Macrothrombocytopenia and Non-syndromic Hearing Loss in a Pediatric Saudi Girl.

A Novel Variant in the DIAPH1 Gene Causing Macrothrombocytopenia and Non-syndromic Hearing Loss in a Pediatric Saudi Girl.

Journal: Cureus
Published: May 25, 2024

A Novel Variant of the LMAN1 Gene in Combined Factor V and Factor VIII Deficiency in a Saudi Female Child: A Case Report.

A Novel Variant of the LMAN1 Gene in Combined Factor V and Factor VIII Deficiency in a Saudi Female Child: A Case Report.

Journal: Cureus
Published: March 24, 2024

Familial Hemophagocytic Lymphohistiocytosis (FHLH) Perforin Deficiency: A Case Study and Literature Review.

Familial Hemophagocytic Lymphohistiocytosis (FHLH) Perforin Deficiency: A Case Study and Literature Review.

Journal: Cureus
Published: March 08, 2024

A Rare MPIG6B Gene Mutation in a Saudi Adolescent Male With Thrombocytopenia, Anemia, and Myelofibrosis: A Case Report.

A Rare MPIG6B Gene Mutation in a Saudi Adolescent Male With Thrombocytopenia, Anemia, and Myelofibrosis: A Case Report.

Journal: Cureus
Published: February 11, 2024

Pulmonary Embolism in an Adolescent With May-Thurner Syndrome: A Case Report.

Pulmonary Embolism in an Adolescent With May-Thurner Syndrome: A Case Report.

Journal: Cureus
Published: October 14, 2023
Showing 1-9 of 9

Last Updated: 09/26/2026