Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Muhammad Ikram Ullah

Rett Syndrome Without MECP2 Mutation in a Pakistani Girl

Life and Science
2020English

Related publications

Rett Syndrome and MeCP2

NeuroMolecular Medicine
Molecular NeuroscienceNeurologyMolecular MedicineCellular
2014English

MECP2 Mutation Interrupts Nucleolin–mTOR–P70S6K Signaling in Rett Syndrome Patients

Frontiers in Genetics
GeneticsMolecular Medicine
2018English

MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome

Neurology
Neurology
2001English

MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches

Journal of Neonatal Biology
2016English

The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders

Pediatric Neurology
Child HealthDevelopmental NeurosciencePediatricsPerinatologyNeurology
2015English

Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome

Journal of Musculoskeletal Disorders and Treatment
2018English

Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome

Journal of Human Genetics
Genetics
2000English

Mosaic MECP2 Variants in Males With Classical Rett Syndrome Features, Including Stereotypical Hand Movements

Clinical Genetics
Genetics
2018English

A Thorough MECP2 Mutation Analysis

Clinical Genetics
Genetics
2008English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy