Results 51 to 60 of about 1,656 (194)

MR imaging findings in primary spinal cord glioblastoma

Radiology Case Reports, 2021
Spinal cord glioblastoma is a rare disease, with an aggressive course and a poor prognosis. We describe magnetic resonance imaging (MRI) findings, in 3 adult cases of biopsy-confirmed glioblastoma.Conventional MRI findings were unclear with regard to the
Paolo Ferrante, MD, Juan Andres Mora, MD, Lourdes Salazar, MD, Elena Martínez Sáez, MD, Cristina Auger, MD, Àlex Rovira, MD   +5 more
doaj   +1 more source

Demyelinating Pseudotumours Presenting as Space Occupying Lesions Mimicking Brain Tumours- A Histopathologic Assessment of Seven Cases [PDF]

Journal of Clinical and Diagnostic Research, 2020
Demyelinating lesions which present as solitary contrast-enhancing masses pose a diagnostic challenge for both radiologists and surgical neuropathologists and can mimic a number of intracranial space occupying lesions either neoplastic/inflammatory ...
B DEEPTHI, SOMASEKHAR POTHULA
doaj   +1 more source

Bilateral abducens nerve palsy in an infant case of fulminant acute disseminated encephalomyelitis: a case report [PDF]

, 2016
BACKGROUND: Sixth (abducens) nerve palsy (ANP) is far less frequent in children and has not been reported as a sign of acute disseminated encephalomyelitis (ADEM). We present an infant case of ADEM with bilateral abducens nerve palsy (BANP).
Guilian Sun, Zhiliang Yang
core   +1 more source

Tumefactive Demyelinating Lesions and Pregnancy

Neurology India, 2019
Until now, only one gestational tumefactive demyelinating lesion (TDL) has been described. Here we report two TDL cases occurring during and after the pregnancy. A 26-year-old 6-week pregnant woman developed a 3-cm left frontotemporoparietal subcortical TDL with inhomogeneous partial enhancement.
Plantone, Domenico, Piantadosi, Carlo, Ruggieri, Serena, Anelli, Vincenzo, Koudriavtseva, Tatiana   +4 more
openaire   +3 more sources

Diagnosis of multiple sclerosis: progress and challenges [PDF]

, 2017
The diagnosis of multiple sclerosis (MS) is based on typical neurological symptoms and signs along with evidence of dissemination of central nervous system (CNS) lesions in space and time.
Brownlee, W, Fazekas, F, Hardy, TA, Miller, DH   +3 more
core   +1 more source

Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases [PDF]

, 2017
How to Cite This Article: Ashrafi Mr, Tavasoli AR, Alizadeh H, Zare Noghabi J, Parvaneh N. Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases. Iran J Child Neurol. Spring 2017; 11(2):69-77.
ALIZADEH, Houman, ASHRAFI, Mahmoud Reza, PARVANEH, Nima, TAVASOLI, Alireza, ZARE NOGHABI, Javad   +4 more
core   +2 more sources

Mutation in RNF170 Causes Unsteady Gait with Hypertrophic Olivary Degeneration

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration resulting from disruption of the Guillain–Mollaret triangle, typically presenting with palatal tremor, ataxia, and nystagmus. Mutations in the Ring Finger Protein 170 (RNF170) gene have been associated with autosomal dominant sensory ataxia.
Change Wang
wiley   +1 more source

Encephalopathy with behavioral and psychiatric features–firstantibody proven case of Anti-NMDA receptor encephalitis from Pakistan [PDF]

, 2015
Background: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is associated with psychiatric symptoms, memory disturbances, seizures, dyskinesia, and catatonia along with other constellation of symptoms.
Khan, Rizwanullah, Memon, Rabel Khalid, Siddiqui, Maimoona   +2 more
core   +1 more source

Clinical Applications of Electrical Conductivity Imaging Using MRI

Journal of Magnetic Resonance Imaging, Volume 63, Issue 5, Page 1224-1245, May 2026.
ABSTRACT Magnetic resonance imaging (MRI) has emerged as a noninvasive technique for probing the electrical properties of biological tissues: electrical conductivity and relative permittivity. This review focuses on the electrical conductivity and provides a comprehensive overview of applications across both low‐ and high‐frequency regimes.
Stefano Mandija, Khin Khin Tha, Nitish Katoch, Cihan Göksu, Ulrich Katscher, Rosalind Sadleir, Kyu‐Jin Jung, Jierong Luo, Ilias I. Giannakopoulos, Dong‐Hyun Kim, Karin Shmueli, Riccardo Lattanzi, Yusuf Ziya Ider, Axel Thielscher, Cornelis van den Berg   +14 more
wiley   +1 more source

A rare case of simple hereditary recessive optic atrophy [PDF]

, 2015
Simple Autosomal Recessive Optic Atrophy (AROA) is a rare hereditary disorder that belongs to a group of disorders called Hereditary Optic Atrophy. Patients diagnosed with simple AROA have complete blindness since birth or from first few months of life ...
Arain, Fazal M., Chand, Prem, Choudary, Tanveer A.   +2 more
core   +1 more source