نتایج جستجو برای: neurometabolic disorder

تعداد نتایج: 597203  

Journal: :Arquivos brasileiros de oftalmologia 2009
Ricardo Evangelista Marrocos de Aragão Régia Maria Gondim Ramos Felipe Bezerra Alves Pereira Andreya Ferreira Rodrigues Bezerra Daniel Nogueira Fernandes

Tay-Sachs disease is an autosomal recessive disorder of sphingolipid metabolism, caused by enzyme hexosaminidase A deficiency that leads to an accumulation of GM2 in neurocytes which results in progressive loss of neurological function. The accumulation of lipid in retinal ganglion cells that leads to a chalk-white appearance of the fundus called 'cherry red spot' is the hallmark of Tay-Sachs d...

2015
Mahmoudreza ASHRAFI Alireza TAVASOLI Omid ARYANI Mohammad VAFAEE-SHAHI

Introduction Canavan disease (CD) is a type of vacuolating leukodystrophy with autosomal recessive inheritance (1). This neurodegenerative disorder is caused by a defect in the aspartoacylase (ASPA) gene encoding the critical enzyme aspartoacylase, which has the role of hydrolyzing N-acetyl-L-aspartic acid (NAA) and providing the acetyl group to oligodendrocytes for myelin synthesis (2, 3). Asp...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children’s hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran narjes jafari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children’s hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran habibeh nejad biglari 2. pediatric neurology department, mofid children’s hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran sayena jabbehdari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran simin khayat zadeh 2. pediatric neurology department, mofid children’s hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran farzad ahmad abadi 3. pediatric neurologist, ardabil university of medical sciences, ardabil, iran

how to cite this article: karimzadeh p, jafari n, nejad biglari h, jabbehdari j, khayat zadeh s, ahmad abadi f, lotfi a. neurometabolic diagnosis in children who referred as neurodevelopmental delay (a practical criteria, in iranian pediatric patients). iran j child neurol. summer 2016; 10(3):73-81.   objective we aimed to investigate the clinical and para clinical manifestations of neuro metab...

2016
Taraka R. Donti Gerarda Cappuccio Leroy Hubert Juanita Neira Paldeep S. Atwal Marcus J. Miller Aaron L. Cardon V. Reid Sutton Brenda E. Porter Fiona M. Baumer Michael F. Wangler Qin Sun Lisa T. Emrick Sarah H. Elsea

Adenylosuccinate lyase (ADSL) deficiency is a rare autosomal recessive neurometabolic disorder that presents with a broad-spectrum of neurological and physiological symptoms. The ADSL gene produces an enzyme with binary molecular roles in de novo purine synthesis and purine nucleotide recycling. The biochemical phenotype of ADSL deficiency, accumulation of SAICAr and succinyladenosine (S-Ado) i...

2015
Cátia F. Lourenço Ana Ledo Cândida Dias Rui M. Barbosa João Laranjinha

The functional and structural integrity of the brain requires local adjustment of blood flow and regulated delivery of metabolic substrates to meet the metabolic demands imposed by neuronal activation. This process-neurovascular coupling-and ensued alterations of glucose and oxygen metabolism-neurometabolic coupling-are accomplished by concerted communication between neural and vascular cells. ...

2017
Aya Goji Hiromichi Ito Kenji Mori Masafumi Harada Sonoka Hisaoka Yoshihiro Toda Tatsuo Mori Yoko Abe Masahito Miyazaki Shoji Kagami

PURPOSE Proton magnetic resonance spectroscopy (1H MRS) is a noninvasive neuroimaging method to quantify biochemical metabolites in vivo and it can serve as a powerful tool to monitor neurobiochemical profiles in the brain. Asperger's syndrome (AS) is a type of autism spectrum disorder, which is characterized by impaired social skills and restrictive, repetitive patterns of interest and activit...

Journal: :Neurology, Neuropsychiatry, Psychosomatics 2019

Journal: :Journal of Clinical Pathology 1964

2016
Dominique Endres Ludger Tebartz van Elst Bernd Feige Stephan Backenecker Kathrin Nickel Anna Bubl Thomas Lange Irina Mader Simon Maier Evgeniy Perlov

In neuropsychiatric research, the aspects of sex have received increasing attention over the past decade. With regard to the neurometabolic differences in the prefrontal cortex and the cerebellum of both men and women, we performed a magnetic resonance spectroscopic (MRS) study of a large group of healthy subjects. For neurometabolic measurements, we used single-voxel proton MRS. The voxels of ...

Journal: :Applied sciences 2021

Despite extensive research, the exact pathomechanisms associated with epileptic seizure formation and propagation have not been elucidated completely. Two-photon imaging (2PI) is a fluorescence-based microscopy technique that, over years, has used to evaluate seizures epilepsy. Here, we review previous applications of 2PI in A systematic search was performed multiple literature databases. We id...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید