Results 161 to 170 of about 64,847 (299)

Polyneuritis cranialis combined with Horner's syndrome: a rare variant of Guillain Barré syndrome. [PDF]

BMC Neurol
Nie X, He W, Qi W, Ma Y, Zhu G, Hao L, Guo X.   +6 more
europepmc   +1 more source

Positive Effects of Caffeine Therapy in a Girl with PDE2A‐Related Paroxysmal Dyskinesia

Movement Disorders Clinical Practice, EarlyView.
Katerina Bernardi, Moritz Thiel, Anne Koy   +2 more
wiley   +1 more source

Incomplete Presentations in Typical Chronic Inflammatory Demyelinating Polyneuropathy: A Single‐Center, Retrospective Study

Muscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Incomplete forms of typical chronic inflammatory demyelinating polyneuropathy (CIDP) have recently been described, but their frequency and clinical characteristics are uncertain. This study aimed to describe a cohort of patients with incomplete typical CIDP.
Young Gi Min, Irad Ahmed, Christina Englezou, Yusuf A. Rajabally   +3 more
wiley   +1 more source

Clinical and Etiological Spectrum of Third, Fourth, Sixth, and Seventh Cranial Nerve Palsies: A Hospital-Based Cross-Sectional Study. [PDF]

Cureus
Verma V, Singh P, Karkhur S, Verma M.
europepmc   +1 more source

Adult‐Onset Dystonia‐Parkinsonism: Do Not Forget SERAC1

Movement Disorders Clinical Practice, EarlyView.
Giulia Scacciatella, Costanza Masetti, Vidal Yahya, Mauro Treddenti, Gaia Oggioni, Tommaso Bocci, Laura Campiglio, Manuela Zardoni, Chiara Rosci, Marta Pengo, Chiara Manfredi, Roberto Del Bo, Edoardo Monfrini, Alessio Di Fonzo, Maurizio Inghilleri, Alberto Priori   +15 more
wiley   +1 more source

Prognosis of Dysphagia in Pediatric Patients With Vocal Fold Immobility

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective This study aims to determine the incidence and prognosis of dysphagia in pediatric patients with true vocal fold (TVF) immobility or hypomobility. Study Design A single‐center retrospective chart review. Setting A single‐institution tertiary‐care center.
Rachel Georgopoulos, Khashayar Arianpour, Samantha Anne   +2 more
wiley   +1 more source

Wilms Tumor in Children with AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala, Jaclyn Schienda, Andrew J. Murphy, Basil Hashimi, Taylor Perry, Nicholas Cost, Junne Kamihara, Elizabeth A. Mullen, Teresa Santiago, Marcus M. Malek   +9 more
wiley   +1 more source

Isolated cranial nerve disorder as presenting sign in multiple sclerosis: optic nerve versus "the others". [PDF]

Front Neurol
Di Stadio A, Scribani Rossi P, Kaski D, Zilli C, Ralli M, Bernitsas E, Altieri M.   +6 more
europepmc   +1 more source

Relationship between Characteristics and Length of Hospitalization of Patient Emergency Hospitalized for Cranial Nerve Disease

, 2011
Kouhei Kajiwara, Masato Kojima, Yuji Koga, Aki KIYOTA   +3 more
openalex   +2 more sources

MPO-ANCA-Associated Hypertrophic Pachymeningitis Mimicking IgG4-Related Disease: A Case Report and Literature Review. [PDF]

J Inflamm Res
Chen Y, Liu L, Xie C.
europepmc   +1 more source