Ischemic stroke in a pediatric patient with very rare coexistence of sickle‐cell/β‐thalassemia and neurofibromatosis type 1-Reference-Cited by-同舟云学术

Ischemic stroke in a pediatric patient with very rare coexistence of sickle‐cell/β‐thalassemia and neurofibromatosis type 1

Published:2023-04-14 Issue:9 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Roka Kleoniki¹^ORCID,Solomou Elena²,Glentis Stavros¹,Gavra Maria³,Kokkinou Eleftheria⁴,Rigatou Efthymia¹,Pons Roser⁴,Kattamis Antonis¹

Affiliation:

1. Division of Pediatric Hematology‐Oncology First Department of Pediatrics "Aghia Sophia" Children's Hospital, Full Member of ERN GENTURIS and ERN EUROBLOODNET National and Kapodistrian University of Athens Athens Greece

2. Department of Internal Medicine University of Patras Medical School Patras Greece

3. Department of CT and MRI "Aghia Sophia" Children's Hospital Athens Greece

4. Pediatric Neurology Unit First Department of Pediatrics "Aghia Sophia" Children's Hospital National and Kapodistrian University of Athens Athens Greece

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30364

Reference12 articles.

1. HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype‐phenotype correlation

2. Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 1

3. Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

4. National Center for Biotechnology Information.ClinVar; [VCV000068317.4] hwnnngcvVaS 2020).National Center for Biotechnology Information. Accessed February 28 2023.https://www.ncbi.nlm.nih.gov/clinvar/variation/VCV000068317.4

5. Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain