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Publications by Mongkon Charoenpitakchai

A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome

Case Reports in Neurological Medicine

English

Related publications

Cancer Risk in Patients With Noonan Syndrome Carrying a PTPN11 Mutation

European Journal of Human Genetics

English

Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome

Journal of Pediatrics

English

Response to Growth Hormone Therapy in Children With Noonan Syndrome: Correlation With or Without PTPN11 Gene Mutation

Hormone Research in Paediatrics

English

Neurodevelopmental Stimulation of a Child With a Noonan Syndrome With a Non-Frequent Mutation in RAF1 Gene — Case Report

The Journal of Neurological and Neurosurgical Nursing

English

First Case of Congenital Myeloproliferative Disorder in a Newborn Diagnosed With Noonan Syndrome

Journal of Neonatal Biology

English

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American Journal of Human Genetics

English

Noonan Syndrome: Comparing Mutation-Positive With Mutation-Negative Dutch Patients

Molecular Syndromology

English

An Atypical Case of Noonan Syndrome With KRAS Mutation Diagnosed by Targeted Exome Sequencing

Annals of Pediatric Endocrinology and Metabolism

English

Septal Myectomy for Severe Neonatal Hypertrophic Cardiomyopathy Caused by PTPN11 Gene Mutation: A Case Report

Biomedical Journal of Scientific & Technical Research

English