Results 81 to 90 of about 4,841 (226)

"Congenital Sensory Neuropathy as a Differential Diagnosis for Phagocytic Immunodeficiency "

open access: yesIranian Journal of Allergy, Asthma and Immunology, 2006
There are few reports about congenital indifference to pain or Hereditary and Sensory Autonomic Neuropathy (HSAN). Several investigations for pathophysiology of this syndrome have been performed and different classifications about it.
Mohammad Gharagozlou   +3 more
doaj  

Clinical applications of immunoglobulin in neuromuscular diseases: focus on inflammatory myopathies [PDF]

open access: yes, 2014
During recent years, an increasing number of neuromuscular diseases have been recognized either to be caused primarily by autoimmune mechanisms, or to have important autoimmune components.
Oliveira, Acary Souza Bulle   +2 more
core   +3 more sources

Conductive Hydrogel‐Enabled Electrode for Scalp Electroencephalography Monitoring

open access: yesSmall Methods, EarlyView.
Conductive hydrogels are emerging as effective EEG electrode‐scalp interfaces to overcome hair barriers. This review presents the demanding parameters for hair‐compatible hydrogel electrodes and summarizes their applications in healthcare and brain‐computer interfaces.
Zichong Ji   +14 more
wiley   +1 more source

Hereditary sensory and autonomic neuropathy type V: Report of a rare case

open access: yesContemporary Clinical Dentistry, 2015
Hereditary sensory and autonomic neuropathy (HSAN) type V is a rare inherited disease caused by a mutation in the neurotrophic tyrosine kinase receptor, type 1 gene located on chromosome 1 (1q21-q22).
Ritesh Kalaskar, Ashita Kalaskar
doaj   +1 more source

Emerging Triboelectric Nanogenerators for In‐Body Implantation

open access: yesSmall Methods, EarlyView.
This review explores functional implantable triboelectric nanogenerators in biomedical applications, discussing their mechanisms, electricity generation, and design approaches. To solve postimplantation challenges, four types of triboelectric nanogenerators (TENGs) are introduced: stretchable, bioadhesive, on‐demand biodegradable, and multiresponsive ...
Xiao Xiao   +4 more
wiley   +1 more source

Congenital Insensitivity to Pain

open access: yesOnline Journal of Health & Allied Sciences, 2011
Congenital Insensitivity to Pain belongs to the family of Hereditary Sensory and Autonomic Neuropathies (HSAN). It is a rare disorder of unknown etiology associated with loss of pain sensation.
Praveen Kumar B,   +2 more
doaj  

Chinese Clinical Practice Guidelines for Auditory Neuropathy (gCAN)

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Auditory neuropathy (AN) is an auditory disorder that affects the function of the auditory pathway. An increasing number of AN cases have been identified with the revelation of the underlying mechanisms, the advancements of diagnostic and detecting techniques.
Chinese Multi‐Center Research Collaborative Group on Clinical Diagnosis and Intervention of Auditory Neuropathy; Editorial Board of Chinese Journal of Otorhinolaryngology Head and Neck Surgery; Society of Otorhinolaryngology Head and Neck Surgery   +43 more
wiley   +1 more source

Scans for signatures of selection in Russian cattle breed genomes reveal new candidate genes for environmental adaptation and acclimation [PDF]

open access: yes, 2018
Domestication and selective breeding has resulted in over 1000 extant cattle breeds. Many of these breeds do not excel in important traits but are adapted to local environments.
A Talenti   +108 more
core   +5 more sources

The Cost of Love: Emotional Labour and Moral Tensions in the Lives of Chinese Young Carers

open access: yesThe British Journal of Sociology, EarlyView.
ABSTRACT Like adults, children also provide care. This article explores the emotional labour of young carers who care for ill or disabled family members in China, a context where children's caregiving remains largely invisible in both policy and scholarship.
Kefan Xue, Kaidong Guo
wiley   +1 more source

A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated [PDF]

open access: yes, 2018
Hereditary sensory neuropathy type 1 (HSAN I) is an autosomal dominant inherited neurodegenerative disorder of the peripheral nervous system associated with mutations in the SPTLC1 subunit of the serine palmitoyltransferase (SPT). Four missense mutations
Hornemann, Thorsten   +7 more
core  

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