Ebru Keskin-Yilmaz

Turkey

Last Updated: 09/26/2026

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Found 14 publications

MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura.

MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura.

Journal: Journal of pediatric hematology/oncology

Published: July 26, 2021

COVID-19-associated multisystem inflammatory syndrome in children: Experiences of three centres in Turkey.

COVID-19-associated multisystem inflammatory syndrome in children: Experiences of three centres in Turkey.

Journal: Modern rheumatology

Published: April 16, 2021

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: February 07, 2020

An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment.

An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment.

Journal: The Turkish journal of pediatrics

Published: January 18, 2020

Missed Diagnosis of β-Thalassemia Trait in Premarital Screening Due to Accompanying HbA2-Yialousa (HBD: c.82G>T).

Missed Diagnosis of β-Thalassemia Trait in Premarital Screening Due to Accompanying HbA2-Yialousa (HBD: c.82G>T).

Journal: Journal of pediatric hematology/oncology

Published: November 06, 2019

A Rare Cause of Cyanosis Since Birth: Hb M-Iwate

A Rare Cause of Cyanosis Since Birth: Hb M-Iwate

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: July 23, 2019

Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association.

Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association.

Journal: Nephron

Published: January 14, 2019

First Report of an SH2D1A Mutation Associated with X-Linked Lymphoproliferative Disease in Turkey

First Report of an SH2D1A Mutation Associated with X-Linked Lymphoproliferative Disease in Turkey

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: February 03, 2018

First Observation of Hemoglobin San Diego, a High Oxygen Affinity Hemoglobin Variant, in Turkey.

First Observation of Hemoglobin San Diego, a High Oxygen Affinity Hemoglobin Variant, in Turkey.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: August 24, 2017

Association between Maternal and Infantile Markers of Cobalamin Status During the First Month Post-Delivery.

Association between Maternal and Infantile Markers of Cobalamin Status During the First Month Post-Delivery.

Journal: Indian journal of pediatrics

Published: August 10, 2017

The role of Matriptase-2 during the early postnatal development in humans.

The role of Matriptase-2 during the early postnatal development in humans.

Journal: Haematologica

Published: January 24, 2016

Iron-refractory iron deficiency anemia.

Iron-refractory iron deficiency anemia.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: March 26, 2015

Showing 1-12 of 14

Last Updated: 09/26/2026