Results 1 to 10 of about 6,021 (155)
Lyme Disease Presenting With Interesting Neurological Features of Weakness and Hyporeflexia: A Case Report [PDF]
Cureus, 2023 Lyme disease is a tick-borne bacterial infection caused primarily by three pathogenic species of spirochete Borrelia (B. burgdorferi, B. afzelii, and B. garinii). It has a wide range of clinical manifestations ranging in severity. Although, it is generally divided into three phases: early localized, early disseminated, and late disease.
Mehak Semy +2 more
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Idiopathic Segmental Anhidrosis with Hyporeflexia: Incomplete Ross Syndrome [PDF]
Journal of the Korean Neurological Association, 2015 Received March 31, 2015 Revised June 4, 2015 Accepted June 4, 2015 Address for correspondence: Hyun Ah Kim, MD Department of Neurology, Keimyung University School of Medicine 56 Dalseong-ro, Jung-gu, Daegu 41931, Korea Tel: +82-53-250-7475 Fax: +82-53-250-7840 E-mail: kha0206@dsmc.or.kr 후천분절무한증(aquired segmental anhidrosis)은 보상성 편측 다한증(hyperhidrosis ...
Min Sung Kang +3 more
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Brazilian Journal of Otorhinolaryngology, 2016 The vestibular evoked myogenic potential is a potential of mean latency that measures the muscle response to auditory stimulation. This potential can be generated from the contraction of the sternocleidomastoid muscle and also from the contraction of extraocular muscles in response to high-intensity sounds.
Tatiana Rocha Silva +2 more
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Indian journal of dermatology, venereology and leprology, 2007 A 39-year-old soldier presented with anhidrosis affecting both upper extremities below the shoulders, the right side of the trunk below the third rib in front and the third vertebra on the back, and the left lower extremity below the inguinal ligament since 1992.
M. P. S. Sawhney, Y K Sharma, Nitu Singh
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HYPOREFLEXIA, HYPOTONIA, AND HYPONATREMIA: A CASE OF GUILLAIN-BARRÉ SYNDROME AND SIADH [PDF]
Chest, 2019 Daniel O. Griffin, Hussein Asad
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SPG10 is a rare cause of spastic paraplegia in European families [PDF]
, 2008 Background: SPG10 is an autosomal dominant form of hereditary spastic paraplegia (HSP), which is caused by mutations in the neural kinesin heavy chain KIF5A gene, the neuronal motor of fast anterograde axonal transport.
Auer-Grumbach, M. +10 more
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Intralabyrinthine Vestibular Schwannoma Responsive to Intratympanic Gentamicin Treatment [PDF]
, 2017 Intralabyrinthine schwannoma (ILS) is a rare benign tumor that affects the ends of cochlear and vestibular nerves. In a majority of the cases, it occurs with unilateral progressive sensorineural hearing loss.
Barbara, Maurizio +6 more
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Vestibular schwannoma and ipsilateral endolymphatic hydrops: an unusual association [PDF]
, 2017 Vestibular schwannoma and endolymphatic hydrops are two conditions that may present with similar audio-vestibular symptoms. The association of the two in the same patient represents an unusual nding that may lead clinicians to errors and delays in ...
ALTISSIMI, Giancarlo +8 more
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Ancient Schwannoma of the Cauda Equina: our experience and review of the literature [PDF]
, 2016 Ancient schwannomas (AS) are exceedingly rare variant of common schwannomas (CS). Only two cases involving the cauda equina region have been previously reported in literature.
Caruso, Riccardo +5 more
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