Suchergebnisse - "Rahman, Omar"

PubPharm (28)

1

Remission of Ectopic Cushing Syndrome Secondary to Medullary Thyroid Cancer With Vandetanib and Selpercatinib

enthalten in: JCEM case reports | 2024

von Jazdarehee, A. | Abdel-Rahman, O. | Jacquier, J.

2

Elbow Osteochondral Allograft Transplantation and Lateral Ulnar Collateral Ligament Repair with Internal Brace : A Case Report

enthalten in: JBJS case connector | 2022

von Lee, S. | Bedford, B. | Kim, A. | +2

3

Elbow ulnar collateral ligament reconstruction using suture tape augmentation

enthalten in: JSES reviews, reports, and techniques | 2021

von Lee, S. | Rabinovich, R. | Rahman, O. | +1

4

Mycobacterium mucogenicum meningitis due to external ventricular drain

enthalten in: Access microbiology | 2020

von Moiz, S. | Rahman, O. | Morcos, M. | +2

5

Congenital Amegakaryocytic Thrombocytopenia : A Case Series Indicating 2 Founder Variants in the Mississippi Band of Choctaw Indians

enthalten in: Journal of pediatric hematology/oncology | 2017

von Newman, L. | Luter, M. | Davis, D. | +3

6

MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death

enthalten in: Genome medicine | 2016

von Eldomery, M. | Akdemir, Z. | Vögtle, F. | +29

7

Sphenoidal esthesioneuroblastoma treated with sequential chemo radiotherapy : a case report and review of the literature

enthalten in: Journal of cancer research and therapeutics | 2014

von Abdel-Rahman, O. | Kamal, K.

8

Index of suspicion. Case 1 : fever, diarrhea, jaundice, and confusion in an 18-year-old male. Case 2: severe anemia in a 6-month-old girl. Case 3: red urine in a 4-month-old boy

enthalten in: Pediatrics in review | 2014

von Ku, E. | Thomas, M. | Ho, C. | +6

9

A new leukocyte hyperadhesion syndrome of delayed cord separation, skin infection, and nephrosis

enthalten in: Pediatrics | 2014

von Simpson, B. | Hogg, N. | Svensson, L. | +4

ErratumIn: Pediatrics. 2014 Apr;133(4):754

10

FOXP1 mutations cause intellectual disability and a recognizable phenotype

enthalten in: American journal of medical genetics. Part A | 2013

von Le Fevre, A. | Taylor, S. | Malek, N. | +10