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First published 2010-12

Novel Neurotrophic Tyrosine Kinase Receptor Type 1 Gene Mutation Associated With Congenital Insensitivity to Pain With Anhidrosis

Yi-Pei Lin, Yi-Ning Su, Wen-Chin Weng [...]

Journal of Child Neurology

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Research article

First published 1992-10

Nonprogressive Type II Hereditary Sensory Autonomic Neuropathy: A Homogeneous Clinicopathologic Entity

Gerard Ferrière, Francesco Guzzetta, Sophie Kulakowski [...]

Journal of Child Neurology

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Research article

First published 1993-07

Unique Hereditary Serisory and Autonomic Neuropathy With Growth Hormone Deficiency

Ruth M. Liberfarb, Anthony H. Jackson, Roland D. Eavey [...]

Journal of Child Neurology

Open access

Review article

First published 2024

Congenital insensitivity to pain with anhidrosis: a literature review and the advocacy for stem cell therapeutic interventions

Muhammad Ikrama, Muhammad Usama, Muhammad Hassan Haider [...]

Therapeutic Advances in Rare Disease

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Research article

First published 2022-1

Population Study of Hand and Wrist Manifestations of Congenital Insensitivity to Pain

Michelle Spiteri, Maximillian Mifsud, Thomas Azzopardi [...]

HAND

Open access

Research article

First published 2017-4

Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis

Ting Wang, Haibo Li, Jingjing Xiang [...]

Journal of International Medical Research

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First published 1995-11

Demyelinating Peripheral Neuropathy in Merosin-Deficient Congenital Muscular Dystrophy

Zamir Shorer, Joanne Philpot, Francesco Muntoni [...]

Journal of Child Neurology

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Research article

First published 2014-7

Recurrent Digital Infections and Osteomyelitis in Monozygotic Twins With Congenital Analgesia and Compulsive Onychophagia

Matthew L. Iorio, John R. Barbour

Journal of Child Neurology

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First published 2005-02

Type I Spinal Muscular Atrophy Can Mimic Sensory-Motor Axonal Neuropathy

Evdokia Anagnostou, Steven P. Miller, Marie-Christine Guiot [...]

Journal of Child Neurology

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Research article

First published 2014-02

Carrier Rates of Four Single-Gene Disorders in Croatian Bayash Roma

Ana Barešić, Marijana Peričić Salihović

Genetic Testing and Molecular Biomarkers

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