Results 51 to 60 of about 9,576 (247)

Hereditary Sensory and Autonomic Neuropathy Type IV in 9 Year Old Boy: A Case Report [PDF]

, 2016
How to Cite This Article: Azadvari M, Emami Razavi SZ, Kazemi Sh. Hereditary Sensory and Autonomic Neuropathy Type IV in 9 Year Old Boy: A Case Report. Iran J Child Neurol.
AZADVARI, Mohaddeseh, EMAMI RAZAVI, Seyedeh Zahra, KAZEMI, Shahrbanoo   +2 more
core   +2 more sources

Ionic–Bionic Interfaces: Advancing Iontronic Strategies for Bioelectronic Sensing and Therapy

Advanced Science, EarlyView.
Ionic–bionic interfaces for bioelectronics leverage ions as multifunctional mediators that combine mechanical compliance, ionic and electronic functionalities, and therapeutic effects. These systems offer real‐time biosignal transduction, effective wound dressing, responsive drug delivery, and seamless interaction between soft tissues and electronic ...
Yun Goo Ro, Yoojin Chang, Jeeyoon Kim, Seungjae Lee, Sangyun Na, Cheolhong Park, Hyunhyub Ko   +6 more
wiley   +1 more source

An Alternative Aproach of Exercise Prescription for Type 2 Diabetes Control in Time and Space Restrictions

Chronic Diseases and Translational Medicine, EarlyView.
Continuum of physical behavior changes and important questions about exercise prescription approach in the diabetes context. ABSTRACT Although physical exercise is widely recognized for its role in glycemic control and overall health, population characteristics such as comorbidities, sedentary behavior, disease‐related complications, and socioeconomic ...
Rodrigo Sudatti Delevatti, Samara Nickel Rodrigues, Cristine Lima Alberton   +2 more
wiley   +1 more source

Hereditary sensory autonomic neuropathy and anaesthesia - a case report

Indian Journal of Anaesthesia, 2007
The hereditary sensory and autonomic neuropathies are a rare group of disorders characterized by progressive loss of function that predominantly affects the peripheral sensory nerves.
Nandini Dave, Anil Sonawane, Sachin Chandolkar   +2 more
doaj  

Hereditary sensory autonomic neuropathy type VI in the age of genetic testing

Annals of the Child Neurology Society
Background Hereditary sensory and autonomic neuropathy type VI (HSAN VI) is a rare recessive genetic disorder caused by mutations in the human dystonin (DST) gene.
Lekshmi Peringassery Sateesh, Pavani Chitamanni, Danielle Akinsanmi, Suman Ghosh, Steven G. Pavlakis, Alexandra Reznikov   +5 more
doaj   +1 more source

The association between neural crest‐derived glia and melanocyte lineages throughout development and disease

Developmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient cell population that emerges from the dorsal neural tube during neurulation and migrates extensively throughout the embryo. Among their diverse derivatives, glial cells (such as Schwann and satellite ganglionic cells) and melanocytes represent two major lineages. In vitro studies suggested they share a common
Chaya Kalcheim
wiley   +1 more source

Cerebellar ataxia and sensory ganglionopathy associated with light-chain myeloma. [PDF]

, 2017
BACKGROUND: Cerebellar ataxia with sensory ganglionopathy is a rare neurological combination that can occur in some hereditary ataxias including mitochondrial diseases and in gluten sensitivity. Individually each condition can be a classic paraneoplastic
A Kumar, A Ramirez-Zamora, A Sghirlanzoni, A Wavre, C Denier, D Hilleman, F Graus, F Scaravilli, J Dalmau, J Dalmau, KG Gwathmey, M Hadjivassiliou, M Hadjivassiliou, M Pavan, P Zis, PD Shanmugarajah, PH Green, S Currie, T Alam   +18 more
core   +2 more sources

Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation [PDF]

Brain, 2009
Hereditary sensory and autonomic neuropathies (HSAN) are clinically and genetically heterogeneous disorders characterized by axonal atrophy and degeneration, exclusively or predominantly affecting the sensory and autonomic neurons. So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and ...
Kilic, SARA ŞEBNEM, Timmerman, Vincent, De Jonghe, Peter, Jordanova, Albena, Kruyt, Moyo C., Swinkels, Marielle, Nascimento, Andres, Weis, Joachim, Bonello-Palot, Nathalie, Levy, Nicolas, Auer-Grumbach, Michaela, Jacobs, An, De Vriendt, Els, Baets, Jonathan, Rotthier, Annelies   +14 more
openaire   +5 more sources

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source

End-Stage Renal Disease in Familial Amyloidosis ATTR Val30Met: A [PDF]

, 2003
Transplant Proc. 2003 May;35(3):1116-20. End-stage renal disease in familial amyloidosis ATTR Val30Met: a definitive indication to combined liver-kidney transplantation.
Beirão, I., Henriques, A.C., Lobato, L., Miranda, H.P., Pereira, M.C., Sarmento, A.M., Seca, R., Teixeira, M., Ventura, A.   +8 more
core