Results 71 to 80 of about 17,135 (242)

Pathological Studies and Postmortem Computed Tomography of Dolphins with Meningoencephalomyelitis and Osteoarthritis Caused by Brucella ceti

Oceans, 2022
Cetacean neurobrucellosis is a common cause of strandings in Costa Rica diagnosed by serology, bacteriology, and histopathology. Pathological studies were performed on 18 dolphins.
Andrés Granados-Zapata, María José Robles-Malagamba, Rocío González-Barrientos, Brian Chin-Wing Kot, Elías Barquero-Calvo, Minor Cordero-Chavaría, Marcela Suárez-Esquivel, Caterina Guzmán-Verri, Jose David Palacios-Alfaro, Connie Tien-Sung, Edgardo Moreno, Gabriela Hernández-Mora   +11 more
doaj   +1 more source

Incidence of toxoplasmosis in pregnancy in Campania: A population-based study on screening, treatment, and outcome [PDF]

, 2019
INTRODUCTION: The aim of this study was to evaluate the incidence of toxoplasmosis infection during pregnancy and to describe the characteristics of the serological status, management, follow-up and treatment.
Agangi, Annalisa, Berghella, Vincenzo, Donadono, Vera, Esposito, Giuseppina, Martinelli, Pasquale, Maruotti, Giuseppe Maria, Mazzarelli, Laura Letizia, Migliorini, Sonia, Quaglia, Filomena, Saccone, Gabriele, Sarno, Laura, Sirico, Angelo, Tagliaferri, Salvatore, Ward, Andrew, Zullo, Fulvio   +14 more
core   +1 more source

Fetal Ventriculomegaly [PDF]

American Journal of Obstetrics and Gynecology, 2020
Mary E, Norton, Nathan S, Fox, Ana, Monteagudo, Jeffrey A, Kuller, Sabrina, Craigo   +4 more
openaire   +2 more sources

FXTAS and the Spectrum of FMR1 Premutation‐Associated Phenotypes in Latin America: A Scoping Review

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Fragile X–associated tremor/ataxia syndrome (FXTAS) is a late‐onset neurodegenerative disorder caused by FMR1 premutation expansions (55–200 CGG repeats). Although well described in populations of predominantly European ancestry, FXTAS remains poorly characterized in Latin America due to limited awareness, restricted access to ...
Amy Schmidmajer, Salomón Páez‐García, Santiago Martínez, Jacobo Ramírez‐Triana, Kevin O'Hara‐Veintimilla, Andrés Ricaurte‐Fajardo, Catalina Cerquera‐Cleves   +6 more
wiley   +1 more source

The Brain‐Age Gap in Pediatric Dystonia: Neuroanatomical Deviations Inform Deep Brain Stimulation Outcomes

Movement Disorders, EarlyView.
Abstract Background Dystonia in children is a heterogeneous condition with variable response to deep brain stimulation (DBS). Brain‐age gap, a machine learning‐derived metric of structural deviation from norm, may capture signatures that differentiate underlying biotypes and predict outcomes.
Timur H. Latypov, Alexandre Berger, Manuela Mohareb, Karim Mithani, Sara Breitbart, Lindsey M. Vogt, Thiemo Dinger, Inge Meijer, Alexander G. Weil, Alfonso Fasano, Carolina Gorodetsky, George M. Ibrahim   +11 more
wiley   +1 more source

Congenital Myopathies and Muscular Dystrophies: A Single Tertiary Center Experience and Factors Associated With Long‐Term Outcomes

Muscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Data on respiratory, feeding, ambulatory outcomes and prognostic factors for congenital myopathies (CM) and congenital muscular dystrophies (CMD) remain limited. Therefore, in this study, we report the characteristics of a large single‐center cohort of patients with CM and CMD, focusing on long‐term outcomes and aiming to ...
Can Ozlu, Margaret McGurn, Susan Iannaccone, Zurisadai Gonzalez Castillo, Kaitlin Batley   +4 more
wiley   +1 more source

Middle Interhemispheric Variant of Holoprosencephaly – Presenting as Non-Visualized Cavum Septum Pellucidum and An Interhemispheric Cyst in A 19-Weeks Fetus [PDF]

Journal of Clinical and Diagnostic Research, 2015
Middle Interhemispheric variant (MIH) is a rare subtype of holoprosencephaly (HPE), also known as syntelencephaly. We present a case of MIH, which was diagnosed as an interhemispheric cyst on antenatal sonography at 19 weeks, but later diagnosed as MIH ...
Akhila Vasudeva, Shalini S Nayak, Rajagopal Kadavigere, Katta M Girisha, Jyothi Shetty   +4 more
doaj   +1 more source

Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To describe the implementation of whole genome sequencing (WGS) in prenatal diagnostics and outline the national guideline system facilitating this. Methods Clinical guidelines for WGS in prenatal diagnostics were developed and implemented by the Danish Fetal Medicine Society.
Ida Vogel, Lotte Andreasen, Marie Balslev‐Harder, Naja Becher, Anja Ernst, Kasper Gadsbøll, Tina Duelund Hjortshøj, Marie Skov Hvidbjerg, Martin Larsen, Stina Lou, Ida Charlotte Bay Lund, Lars Henning Pedersen, Laura Kirstine Sønderberg Roos, Lene Sperling, Lone Sunde, Pernille Mathiesen Tørring, Cathrine Vedel, Olav Bjørn Petersen   +17 more
wiley   +1 more source

Volumetric MRI Analysis of a Case of Severe Ventriculomegaly

Frontiers in Human Neuroscience, 2018
We present a case of a 60-year-old male referred to a tertiary psychiatric facility for diagnostic assessment due to low mood and behavioral changes. Neurological examination of the patient was unremarkable.
Gésine L. Alders, Luciano Minuzzi, Luciano Minuzzi, Luciano Minuzzi, Sachin Sarin, Benicio N. Frey, Benicio N. Frey, Benicio N. Frey, Geoffrey B. Hall, Zainab Samaan   +9 more
doaj   +1 more source

NORMAL PRESSURE HYDROCEPHALUS: LITERATURE REVIEW

Arta Medica, 2020
Objectives. Normal pressure hydrocephalus is a potentially reversible disease, characterized by a pathological enlargement of the cerebral ventricles, with a normal opening pressure during the lumbar puncture.
Paula Fala, Victor Andronachi, Mihail Gavriliuc, Pavel Gavriliuc, Alexandru Andrușca, Olga Gavriliuc   +5 more
doaj   +1 more source