Results 11 to 20 of about 101,596 (292)
Unilateral RS3PE in a Patient of Seronegative Rheumatoid Arthritis
Case Reports in Rheumatology, 2013 Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) is a rare but well-reported clinical entity. It is classically described as symmetrical involvement of both upper extremities.
Ankur Nandan Varshney +7 more
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Unilateral ocular myasthenia gravis-A case report
Indian Journal of Ophthalmology, 1990 Unilateral ocular myasthenia gravis is being reported. He had significant involvement of one eye with no involvement of the fellow eye.
Chouhan Jugal, Soni Tara, Mishra Y
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Acta Orthopaedica, 2016 Background and purpose — Idiopathic clubfoot can be bilateral or unilateral; however, most studies of gait have assessed clubfoot cases as one uniform group.
Elin Lööf +4 more
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Surgical outcomes in patients with drug-resistant bilateral temporal lobe epilepsy confirmed via magnetic resonance imaging [PDF]
Анналы клинической и экспериментальной неврологии, 2022 Introduction. In patients with drug-resistant temporal lobe epilepsy (TLE), surgical treatment is aimed to resect an epileptogenic zone (EZ) followed by seizure control.
Vladimir V. Krylov +11 more
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The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2023 Background Cerebellar malformations are broadly categorized into hypoplasias and dysplasias, which are further divided based on focal or diffuse involvement. Both hypoplasias and dysplasias are usually associated with cerebral involvement or as a part of
Ruchika Babal, Abhishek Aggarwal
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Unilateral versus bilateral lymph-nodal metastases and oncologic outcome in vulvar cancer patients. [PDF]
, 2020 PURPOSE To evaluate the difference in oncologic outcome between vulvar cancer patients with uni- and bilateral inguino-femoral lymph nodal involvement and to identify factors affecting their oncologic outcome MATERIALS AND METHODS: Patients who ...
Gasparri, Maria Luisa +5 more
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Möbius Syndrome as a Syndrome of Rhombencephalic Maldevelopment: A Case Report
Pediatrics and Neonatology, 2009 Möbius syndrome is a rare congenital disorder characterized by congenital facial weakness with impairment of ocular abduction. It is considered as a rhombencephalic disorder, and is often accompanied with hypoplasia of the pons and cerebellum.
Hsueh-Ting Huang +3 more
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Scientific Reports, 2022 Approximately 25% of glioblastomas show at diagnosis a corpus callosum infiltration, which is associated with poor prognosis. The extent of corpus callosum involvement, however, ranges from partial unilateral to complete bilateral infiltration.
Mohammad Hazaymeh +6 more
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Progress in Orthodontics, 2021 Background There is currently no information on how different mandibular segments are affected by juvenile idiopathic arthritis. The aim of this paper is to assess volumetric differences of different mandibular segments in subjects with unilateral and ...
Davide Cavagnetto +4 more
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An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement [PDF]
, 1981 An 81-year-old man from a family with a history of oculopharyngeal muscular dystrophy (OPMD) involving 6 members over 4 generations is described. The patient first noted drooping of his eyelids at the age of 65.
Krause, Klaus-Henning, Schmitt, H.-P.
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