List of works - Parham Habibzadeh

A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment

scientific article published on 04 September 2019

A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report

scientific article published on 14 January 2019

An immunocompetent patient with a nonsense mutation in NHEJ1 gene

article

Are current archiving systems reliable enough?

scientific article (publication date: 30 July 2015)

Choice of criterion used in the receiver operating characteristic analysis

scientific article published in April 2017

Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series

scientific article published on 29 October 2019

Decay of References to Web sites in Articles Published in General Medical Journals: Mainstream vs Small Journals

scientific article (publication date: 2013)

HDAC Inhibitors Induce Expression and Promote Neurite Outgrowth in Human Neural Progenitor Cells-Derived Neurons ⬇️

scientific article published on 05 March 2019

High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia

scientific article published on 25 September 2021

Looking for the remedies

scientific article published on 16 December 2015

Our red-green world

scientific article published on 19 October 2015

Psychopathic teamwork: lessons learned from recent terrorist attacks

scientific article published on 05 February 2016

Re: Eric A. Klein, Arnon Chait, Jason M. Hafron, et al. The Single-parameter, Structure-based IsoPSA Assay Demonstrates Improved Diagnostic Accuracy for Detection of Any Prostate Cancer and High-grade Prostate Cancer Compared to a Concentration-based

The COVID-19 Emergency Response Should Include a Mental Health Component

scientific article published on 01 April 2020

The Novel Coronavirus: A Bird's Eye View

scientific article published on 05 February 2020

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.

scientific article published in June 2019

List of works by Parham Habibzadeh