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Rare diseases / Developmental neuroscience / Neurochemistry / Programmed cell death / TrkA receptor / Congenital insensitivity to pain with anhidrosis / Hereditary sensory and autonomic neuropathy / Familial dysautonomia / Anhidrosis / Biology / Health / Tyrosine kinase receptors


Document Date: 2008-11-06 22:19:38

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City

Philadelphia / Bandar Tun Razak / Kumamoto / Kuala Lumpur / /

Company

Malaysia I Farah Wahida Tissue Engineering Laboratory / Matsuda / Smith AG / /

Country

Malaysia / Japan / /

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Facility

Hospital Universiti Kebangsaan Malaysia / Medical Research Centre of National University / /

IndustryTerm

chemical predisposition / /

MedicalCondition

deformities / pyruvate kinase deficiency / anhidrosis / hereditary sensory and autonomic neuropathies / disease / RileyDay syndrome / suspected ectodermal dysplasia / mental deficiency / HSAN / familial dysautonomia / chronic ulcers / primary tooth loss / Peripheral neuropathy / hereditary sensory and autonomic neuropathy type IV / pain / rare disorder / learning disabilities / joint deformities / peripheral neuropathies / recurrent fever / chronic eczematous skin / infections / avascular necrosis / /

Movie

The youngest son / /

Organization

Department of Orthopaedics and Traumatology / Faculty of Medicine / National University of Malaysia / Sharaf Department of Orthopaedics and Traumatology / Kumamoto University School of Medicine / Universiti Kebangsaan Malaysia / Kuala Lumpur / Medical Research Centre / Malaysia BHI Ruszymah Department of Physiology / Department of Paediatrics / /

Person

Hassan M. Congenital / Nasir Hassan / Shalimar Abdullah / Yasuhiro Indo / Mother / Vol / /

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Position

WB / /

Product

glycine / /

Technology

DNA sequencing / /

SocialTag