List of works - Ye Jee Shim

A case of inherited type 1 and type 2A von Willebrand disease confirmed by diagnostic exome sequencing

scientific article published on 12 June 2018

A cross-sectional retrospective study to analyze the underlying causes and clinical characteristics of children with reactive thrombocytosis at a Korean tertiary medical center

scholarly article by Juhee Shin et al published September 2018 in Blood research

A novel mutation of congenital factor V deficiency in Henoch-Schönlein purpura

scientific article published on 01 August 2020

Clinical Characteristics and Treatment Outcomes in Children, Adolescents, and Young-adults with Hodgkin's Lymphoma: a KPHOG Lymphoma Working-party, Multicenter, Retrospective Study

scientific article published on 30 November 2020

Clinical characteristics and treatment courses for cytomegalovirus-associated thrombocytopenia in immunocompetent children after neonatal period.

scientific article

Epidemiological Study of Hereditary Hemolytic Anemia in the Korean Pediatric Population during 1997-2016: a Nationwide Retrospective Cohort Study

scientific article published on 24 August 2020

Evaluation of peritoneal capacity for peritoneal dialysis after abdominal surgery.

scientific article published on 9 February 2010

Flow cytometric osmotic fragility testing does reflect the clinical severity of hereditary spherocytosis.

scientific article

Formula fed twin infants with recurrent hypocalcemic seizures with vitamin D deficient rickets and hyperphosphatemia.

scientific article published on 30 June 2015

Genetic classification and confirmation of inherited platelet disorders: current status in Korea

scientific article published on 06 February 2020

Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing

scientific article published on 07 March 2015

Identification of Novel JAK3 Mutations by Whole-Exome Sequencing in a Korean Boy With Severe Combined Immunodeficiency.

scientific article published in June 2017

Korean parents' perception on the challenges and needs at school re-entry during or after childhood and adolescent cancer - A multi-institutional survey by Korean Society of Pediatric Hematology and Oncology (KSPHO)

scientific article published on 06 February 2020

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte

scientific article published on 23 May 2019

Multiple daily injection of insulin regimen for a 10-month-old infant with type 1 diabetes mellitus and diabetic ketoacidosis.

scientific article

Natural course of childhood chronic immune thrombocytopenia using the revised terminology and definitions of the international working group: a single center experience

scientific article

NovelELANEGene Mutation in a Korean Girl with Severe Congenital Neutropenia ⬇️

scientific article published on November 29, 2011

Pharmacokinetics and prophylactic use of FEIBA®in a child with severe congenital factor X deficiency and recurrent spontaneous intracranial haemorrhage: a case report ⬇️

scientific article published on August 1, 2013

Prefixation of neutrophils for neutrophil antibody testing

scientific article published on 01 January 2014

Progress of in vitro factor VIII coagulant activity from 0 to 8 hours after reconstitution.

scientific article

School performance of childhood cancer survivors in Korea: A multi-institutional study on behalf of the Korean Society of Pediatric Hematology and Oncology

scientific article published on 12 July 2018

Second case of postpartum acquired hemophilia A in a Korean female

scientific article

Sequential strategy for umbilical cord blood transplantation in a Korean Fanconi anemia girl with refractory acute myelomonocytic leukemia and complex karyotype.

scientific article published on 15 December 2016

Serum cytokine profiles in infants with infantile hemangiomas on oral propranolol treatment: VEGF and bFGF, potential biomarkers predicting clinical outcomes

scientific article published on 20 April 2020

Short stature and growth hormone deficiency in a girl with encephalocraniocutaneous lipomatosis and Jaffe-Campanacci syndrome: a case report

scientific article published on 31 December 2016

Survival and Prognosis of Patients with Pilocytic Astrocytoma: A Single-Center Study

scientific article published on 01 October 2019

The first Korean case with Floating-Harbor syndrome with a novel SRCAP mutation diagnosed by targeted exome sequencing

scientific article published on 16 September 2018

Thrombocythemia 1 With THPO Variant (c.13+1G>A) Diagnosed Using Targeted Exome Sequencing: First Case in Korea

scientific article published on 01 July 2020

Treatment outcome of pediatric acute lymphoblastic leukemia in Yeungnam region: Multicenter retrospective study of Study Alliance of Yeungnam Pediatric Hematology-Oncology (SAYPH)

scientific article published on 01 May 2018

List of works by Ye Jee Shim

A case of inherited type 1 and type 2A von Willebrand disease confirmed by diagnostic exome sequencing

A cross-sectional retrospective study to analyze the underlying causes and clinical characteristics of children with reactive thrombocytosis at a Korean tertiary medical center

A novel mutation of congenital factor V deficiency in Henoch-Schönlein purpura

Clinical Characteristics and Treatment Outcomes in Children, Adolescents, and Young-adults with Hodgkin's Lymphoma: a KPHOG Lymphoma Working-party, Multicenter, Retrospective Study

Clinical characteristics and treatment courses for cytomegalovirus-associated thrombocytopenia in immunocompetent children after neonatal period.

Epidemiological Study of Hereditary Hemolytic Anemia in the Korean Pediatric Population during 1997-2016: a Nationwide Retrospective Cohort Study

Evaluation of peritoneal capacity for peritoneal dialysis after abdominal surgery.

Flow cytometric osmotic fragility testing does reflect the clinical severity of hereditary spherocytosis.

Formula fed twin infants with recurrent hypocalcemic seizures with vitamin D deficient rickets and hyperphosphatemia.

Genetic classification and confirmation of inherited platelet disorders: current status in Korea

Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing

Identification of Novel JAK3 Mutations by Whole-Exome Sequencing in a Korean Boy With Severe Combined Immunodeficiency.

Korean parents' perception on the challenges and needs at school re-entry during or after childhood and adolescent cancer - A multi-institutional survey by Korean Society of Pediatric Hematology and Oncology (KSPHO)

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte

Multiple daily injection of insulin regimen for a 10-month-old infant with type 1 diabetes mellitus and diabetic ketoacidosis.

Natural course of childhood chronic immune thrombocytopenia using the revised terminology and definitions of the international working group: a single center experience

NovelELANEGene Mutation in a Korean Girl with Severe Congenital Neutropenia ⬇️

Pharmacokinetics and prophylactic use of FEIBA®in a child with severe congenital factor X deficiency and recurrent spontaneous intracranial haemorrhage: a case report ⬇️

Prefixation of neutrophils for neutrophil antibody testing

Progress of in vitro factor VIII coagulant activity from 0 to 8 hours after reconstitution.

School performance of childhood cancer survivors in Korea: A multi-institutional study on behalf of the Korean Society of Pediatric Hematology and Oncology

Second case of postpartum acquired hemophilia A in a Korean female

Sequential strategy for umbilical cord blood transplantation in a Korean Fanconi anemia girl with refractory acute myelomonocytic leukemia and complex karyotype.

Serum cytokine profiles in infants with infantile hemangiomas on oral propranolol treatment: VEGF and bFGF, potential biomarkers predicting clinical outcomes

Short stature and growth hormone deficiency in a girl with encephalocraniocutaneous lipomatosis and Jaffe-Campanacci syndrome: a case report

Survival and Prognosis of Patients with Pilocytic Astrocytoma: A Single-Center Study

The first Korean case with Floating-Harbor syndrome with a novel SRCAP mutation diagnosed by targeted exome sequencing

Thrombocythemia 1 With THPO Variant (c.13+1G>A) Diagnosed Using Targeted Exome Sequencing: First Case in Korea

Treatment outcome of pediatric acute lymphoblastic leukemia in Yeungnam region: Multicenter retrospective study of Study Alliance of Yeungnam Pediatric Hematology-Oncology (SAYPH)