Thais K. Homma

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 17 publications

Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.

Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.

Journal: Clinical genetics

Published: August 30, 2024

Response to Recombinant Human Growth Hormone Therapy in Short Children Born at Very Low Birth Weight.

Response to Recombinant Human Growth Hormone Therapy in Short Children Born at Very Low Birth Weight.

Journal: Hormone research in paediatrics

Published: July 22, 2024

Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature.

Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature.

Journal: Journal of autism and developmental disorders

Published: November 26, 2022

A thermosensitive PCNA allele underlies an ataxia-telangiectasia-like disorder.

A thermosensitive PCNA allele underlies an ataxia-telangiectasia-like disorder.

Journal: The Journal of biological chemistry

Published: November 04, 2022

High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight.

High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight.

Journal: American journal of medical genetics. Part A

Published: February 04, 2022

Noonan syndrome patients beyond the obvious phenotype: A potential unfavorable metabolic profile.

Noonan syndrome patients beyond the obvious phenotype: A potential unfavorable metabolic profile.

Journal: American journal of medical genetics. Part A

Published: September 02, 2020

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome.

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome.

Journal: Endocrine connections

Published: October 28, 2019

Genetic investigation of patients with tall stature.

Genetic investigation of patients with tall stature.

Journal: European journal of endocrinology

Published: October 02, 2019

Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature.

Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature.

Journal: Hormone research in paediatrics

Published: May 28, 2019

Evaluation of SHOX defects in the era of next-generation sequencing.

Evaluation of SHOX defects in the era of next-generation sequencing.

Journal: Clinical genetics

Published: March 29, 2019

Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing.

Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing.

Journal: The Journal of pediatrics

Published: March 09, 2019

Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan Syndrome.

Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan Syndrome.

Journal: Hormone research in paediatrics

Published: October 09, 2018

Showing 1-12 of 17

Last Updated: 09/26/2026