Maryam Kachuei

4PUBLICATIONS
4CO-AUTHORS
Early English languagesNeonatologyInfant and child healthPsychosocial aspects of childbirth and perinatal mental health
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Publications (4)

|Aug 25, 2025
BCKDK gene mutations as a rare condition responsible for comorbid neurodevelopmental delay, autism, and epilepsy: a case series of four patients.

Parvaneh Karimzadeh, Maryam Kachuei, Hossein Najmabadi

|Dec 09, 2024
Eyebrow bleeding as a rare migraine symptom: a case report.

Azita Tavasoli, Mohammad Rezazadeh, Maryam Kachuei

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