Results 51 to 60 of about 9,800 (213)
A case of variant of GBS with positive serum ganglioside GD3 IgG antibody
Italian Journal of PediatricsBackground Acute bulbar palsy-plus (ABPp) syndrome is an unusual variant of Guillain-Barré syndrome (GBS). Anti-GT1a and anti-GQ1b antibodies have been reported in patients with ABPp, but without reports related to GD3 antibodies.
Jiao Xue +7 more
doaj +1 more source
THE PSYCHOMOTOR THEORY OF HUMAN MIND [PDF]
, 2007 This study presents a new theory to explain the neural origins of human mind. This is the psychomotor theory. The author briefly analyzed the historical development of the mind-brain theories.
TAN, Prof. Dr. Uner
core +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Frontiers in Neurology, 2021 Background: Spinal and bulbar muscular atrophy (SBMA) is an X-lined motor neuron disease characterized by progressive muscle weakness, bulbar palsy, and dysphagia.
Dae-Won Gwak +7 more
doaj +1 more source
Recurrent Maxillary Ameloblastoma Presenting as an External Auditory Canal Mass
The Laryngoscope, EarlyView.Ameloblastoma with temporal bone involvement is exceedingly rare, with no prior reports of external auditory canal presentation. This case report demonstrates successful multidisciplinary management with extensive skull base resection and adjuvant radiation therapy, emphasizing the role of proton therapy in achieving tissue‐sparing treatment and long ...
Bailey H. Duhon +5 more
wiley +1 more source
Arquivos de Neuro-Psiquiatria, 2002 A mielinólise pontina central (MPC) e extra-pontina (MEP) é enfermidade desmielinizante do encéfalo associada principalmente com a correção rápida da hiponatremia, que se manifesta principalmente por tetraparesia espástica e paralisia pseudo-bulbar ...
Francisco Manoel B. Germiniani +4 more
doaj +1 more source
Movement Disorders Clinical Practice, EarlyView.ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan +4 more
wiley +1 more source
Atypical MRI features in familial adult onset Alexander disease: case report [PDF]
, 2016 BACKGROUND: Alexander disease (AxD) is a rare neurological disease, especially in adults. It shows variable clinical and radiological features. CASE PRESENTATION: We diagnosed a female with AxD presenting with paroxysmal numbness of the limbs at the ...
Anna Zhou +7 more
core +1 more source
Longitudinal Videofluorographic Dysphagia Measures in Progressive Supranuclear Palsy
Movement Disorders Clinical Practice, EarlyView.Abstract Background Dysphagia can lead to fatal aspiration pneumonia in progressive supranuclear palsy (PSP). Little is known about the longitudinal progression of dysphagia or whether it differs across PSP clinical variants. Objectives To characterize longitudinal changes in dysphagia across PSP variants and determine relationships with disease ...
Anna Chiara Cattani +8 more
wiley +1 more source
Lyme neuroborreliosis in a critically ill patient
The Journal of the International Society of Physical and Rehabilitation Medicine, 2020 Lyme neuroborreliosis (LNB) is a nervous system infection caused by the species of the spirochete Borrelia. A woman, with a history of right facial palsy, was admitted to the physical and rehabilitation medicine (PRM) unit for the rehabilitation of ...
Rui Alexandre Do Prado Costa +3 more
doaj +1 more source