Results 221 to 230 of about 3,345,719 (364)

An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco, Caterina Motta, Enrica Marchionni, Maria Rosaria D'Apice, Carlangelo Carrese, Giuseppe Novelli, Alessandro Martorana, Chiara Giuseppina Bonomi   +7 more
wiley   +1 more source

Trombiculiasis in 4 Dogs with Neurologic Signs, the Netherlands, 2024. [PDF]

Emerg Infect Dis
Santifort KM, Reijmerink HA.
europepmc   +1 more source

Neurological Abnormalities: Their Occurrence and Significance as illustrated by an Examination of 500 Mental Defectives [PDF]

, 1933
R. G. Gordon, Ross Norman, Richard Berry
openalex   +1 more source

ALS With and Without Upper Motor Neuron Signs: A Comparative Study Supporting the Gold Coast Criteria

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The Gold Coast criteria permit diagnosis of amyotrophic lateral sclerosis (ALS) even without upper motor neuron (UMN) signs. However, whether ALS patients with UMN signs (ALSwUMN) and those without (ALSwoUMN) share similar characteristics and prognoses remains unclear.
Hee‐Jae Jung, E‐nae Cheong, Jungmin So, Heung‐Won Kang, Yangsean Choi, Eun‐Jae Lee, Hyunjin Kim, Young‐Min Lim   +7 more
wiley   +1 more source

Dorsal laminectomy for treatment of cervical vertebral stenotic myelopathy in an alpaca [PDF]

Barker, W H J, Driver, C J, Jull, P, Volk, H A, Whitehead, C E, Witte, T H   +5 more
core   +1 more source

The neurological examination technique for toddler-age.

, 1993
M. S. Hempel
openalex   +1 more source

CHARACTERISTICS OF ENMG EXAMINATION IN MORBUS HANSEN PATIENT IN NEUROLOGY POLYCLINIC SANGLAH GENERAL HOSPITAL

, 2020
Putu Nusartha, I Wayan Gede Bandem ARIMBAWA, I Made Dwi Cahya Prayogi Putra, I Putu Eka Widyadharma, Ni Kadek Mira Pratiwi   +4 more
openalex   +1 more source

The Case of a 37‐Year‐Old Woman Presenting With Subacute Weakness and Paresthesias

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Acute intermittent porphyria (AIP) is a rare metabolic disorder that may present with subacute neuropathy and systemic symptoms, often leading to diagnostic delay. We report a 37‐year‐old woman with eight weeks of progressive bilateral upper extremity weakness and paresthesias, followed by lower extremity involvement and falls, in the setting ...
Peter Pacut, Joy Cannon, Neel Dixit, Qihua Fan   +3 more
wiley   +1 more source

A presumptive case of gluten sensitivity in a border terrier: a multisystem disorder? [PDF]

, 2016
BLACK, CATASSI, DAY, GARDEN, GHAZAL, HADJIVASSILIOU, HADJIVASSILIOU, HADJIVASSILIOU, HADJIVASSILIOU, HADJIVASSILIOU, HALL, LOWRIE, SAPONE, SÁRDY, VOLTA, WASHABAU, WILLARD   +16 more
core   +3 more sources

The Case of a 28‐Year‐Old Man With Gradually Progressive Proximal Leg Weakness

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This is a case of a 28‐year‐old man who presented with a 6‐month history of gradually progressive proximal leg weakness and pain that worsened on exercise and was relieved by rest. He had no symptoms in his upper limbs. Apart from intermittent mild ptosis and diplopia, he had no other cranial nerve symptoms.
Melody T. Asukile, Musambo Kapapa, Emelda Mwingila, Michelle Kvalsund   +3 more
wiley   +1 more source