Kitiwan Rojnueangnit

16PUBLICATIONS
22CO-AUTHORS
Neurology and neuromuscular diseasesMajor global burdens of diseaseDevelopmental genetics (incl. sex determination)Optical technologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (16)

|Mar 19, 2026
Early Diagnosis of Nieman-Pick Disease Type C and Rapid Response of Gelastic Cataplexy to Treatment With N-Acetyl-L-Leucine: A Case Report.

Kitiwan Rojnueangnit, Sukita Puttamanee, Sukkrawan Intarakhao

|Mar 16, 2026
Impacts and Economic Burden of Pompe Disease on Patients and Families in Thailand: A Mixed Method Study.

Sitaporn Youngkong, Montarat Thavorncharoensap, Usa Chaikledkaew

|Jul 10, 2024
Comparison of the Accuracy in Provisional Diagnosis of 22q11.2 Deletion and Williams Syndromes by Facial Photos in Thai Population Between De-Identified Facial Program and Clinicians.

Nop Khongthon, Midi Theeraviwatwong, Khunton Wichajarn

|Sep 04, 2023
Microspherophakic Angle Closure Glaucoma in a Patient with Coffin-Siris Syndrome: Case Report.

Kulawan Rojananuangnit, Kitiwan Rojnueangnit

|Oct 20, 2022
Genetic diagnosis for adult patients at a genetic clinic.

Kitiwan Rojnueangnit, Pimjai Anthanont, Thanitchet Khetkham

|Feb 21, 2022
Clinical Features to Predict 22q11.2 Deletion Syndrome Proven by Molecular Genetic Testing.

Kitiwan Rojnueangit, Thanitchet Khetkham, Preyaporn Onsod

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Frequent Collaborators

2 joint publications

Thanitchet Khetkham

2 joint publications

Thipwimol Tim-Aroon

1 joint publications

Takol Chareonsirisuthigul

1 joint publications

Naiyana Boontan