Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Divpreet Kaur"'
Autor:
Mandy Hsu, Nader El Seblani, Zahra Zhu, Bhuvaneswari Ramisetty, Christopher Day, Jikku Zachariah, Divpreet Kaur, Ashutosh Kumar, Sita Paudel, Dustin Paul, Puneet Singh Kochar, Paul R Carney, Sunil Naik
Publikováno v:
Children, Vol 10, Iss 4, p 724 (2023)
Elsberg syndrome is a typically infectious syndrome that may cause acute or subacute bilateral lumbosacral radiculitis and sometimes lower spinal cord myelitis. Patients often present with various neurological symptoms involving the lower extremities
Externí odkaz:
https://doaj.org/article/c82417d6e3e2483b9a70278ba462834f
Publikováno v:
Interdisciplinary Neurosurgery, Vol 5, Iss C, Pp 51-53 (2016)
Pseudomeningocele is a known cause of myelopathy, however this is classically associated with bilateral symptoms. We discuss a patient presenting with single upper extremity weakness, initially diagnoses as monomelic amyotrophy, which further investi
Externí odkaz:
https://doaj.org/article/67db9d8ad47e4c39b1696dfdab5fee2d
Publikováno v:
Child Neurology Open
Child Neurology Open, Vol 9 (2022)
Child Neurology Open, Vol 9 (2022)
Over six billion doses of Coronavirus Disease 2019 (COVID-19) vaccines have been administered worldwide. Amidst the global COVID-19 vaccination campaign, vaccine-related side effects are of ongoing concern and investigation. According to the Centers
Publikováno v:
Lecture Notes in Electrical Engineering ISBN: 9789811623530
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c1d997ddc3ac26279ae68183a19d5c1
https://doi.org/10.1007/978-981-16-2354-7_41
https://doi.org/10.1007/978-981-16-2354-7_41
Autor:
Armineuza Evora, Eric A. Macklin, Adel Marei, P. Davila-Pérez, Seward B. Rutkove, Brian J. Wainger, William S. David, Courtney E. McIlduff, James D. Berry, Joan A. Camprodon, Clifford J. Woolf, Bjorn Oskarsson, Nicholas J. Maragakis, Nazem Atassi, Richard A. Lewis, Richard Bedlack, Sean K. Meehan, Evangelos Kiskinis, Shafeeq Ladha, Alvaro Pascual-Leone, Karissa L. Gable, Matthew C. Kiernan, Aura Hurtado, João D. Pereira, Elizabeth A. Mauricio, Zachary Simmons, Divpreet Kaur, Nicolas Phielipp, Sylvia Baedorf Kassis, Robert H. Baloh, Michael D. Weiss, Kevin Eggan, Merit Cudkowicz, Pablo Celnik, David Klements, Peter B. Rosenquist, Lindsay Pothier, Thuong La, Joan Koh, Meghan Hall, Namita Goyal, Sabrina Paganoni, Steve Vucic, Dale J. Lange, Jeremy M. Shefner, Vern C. Juel, Vinay Chaudhry, Stephen A. Goutman, Michael H. Rivner
Publikováno v:
JAMA Neurol
IMPORTANCE: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of the motor nervous system. Clinical studies have demonstrated cortical and spinal motor neuron hyperexcitability using transcranial magnetic stimulation and
Publikováno v:
MusclenerveREFERENCES. 63(1)
Autonomic neuropathies represent a complex group of disorders that preferentially target autonomic fibers and can be classified as either acute/subacute or chronic in onset. Acute-onset autonomic neuropathies manifest with such conditions as paraneop
Publikováno v:
Clinical Neurology and Neurosurgery. 149:147-153
Sciatic nerve neuropathy due to infiltrating of a high grade B-cell lymphoma is a very rare situation and has not often been reported. We report a case with a previous history of indolent lymphoma who presented with isolated sciatic nerve neuropathy
Publikováno v:
Muscle & Nerve. 54:161-164
The sarcoglycanopathies are a heterogeneous group of autosomal recessive limb-girdle muscular dystrophies that cause varying degrees of progressive proximal muscle weakness.We describe the case of a Caucasian girl who presented with exercise intolera
Publikováno v:
Interdisciplinary Neurosurgery, Vol 5, Iss C, Pp 51-53 (2016)
Pseudomeningocele is a known cause of myelopathy, however this is classically associated with bilateral symptoms. We discuss a patient presenting with single upper extremity weakness, initially diagnoses as monomelic amyotrophy, which further investi
Publikováno v:
Musclenerve. 54(1)
The sarcoglycanopathies are a heterogeneous group of autosomal recessive limb-girdle muscular dystrophies that cause varying degrees of progressive proximal muscle weakness.We describe the case of a Caucasian girl who presented with exercise intolera