Results 311 to 320 of about 2,096,156 (396)

Sourcing and utilization of bodies of the deceased for medical education and research: An examination of West African universities. [PDF]

Anat Sci Educ
Boadum O, Ahenkorah J, Balta JY.
europepmc   +1 more source

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao, Katherine R Schon, Jana Vandrovcova, Özlem Yayıcı Köken, Sharika Raga, Kireshnee Naidu, Maryke Schoonen, Nimita Rani, Pedro Tomaselli, Dipti Baskar, Musambo Kapapa, Ipek Polat, Lindsay A Wilson, Kumarasamy Thangaraj, Uluç Yiş, Bevinahalli N Nandeesh, David Bearden, Michelle Kvalsund, Franclo Henning, Seena Vengalil, Atchayaram Nalini, Claudia F. R. Sobreira, Wilson Marques, Haluk Topoloğlu, Michael G Hanna, Sireesha Yareeda, Venugopalan Y Vishnu, Francois H van der Westhuizen, Izelle Smuts, Surita Meldau, Jo Wilmshurst, Büşranur Çavdarlı, Jeannine Heckmann, Patrick F Chinnery, Rita Horvath   +34 more
wiley   +1 more source

Evaluation of radiological data for three-dimensonal physical models to assist personalized anesthesia in neuroaxial interventions with difficult anatomy. [PDF]

Medicine (Baltimore)
Cagiran Z, Cagiran I, Karaman S, Govsa F, Ozer MA, Sertoz N.   +5 more
europepmc   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala   +17 more
wiley   +1 more source

Innovative sphincterotomy knife and indigo carmine strategy for bile duct stones in a patient with surgically altered anatomy. [PDF]

Endoscopy
Soga K, Sakakibara K, Soma Y, Hayakawa F, Yamaguchi M, Kobori I, Tamano M.   +6 more
europepmc   +1 more source

Development and Validation of two Bronchoscopy Knowledge Assessments.

Respiration
Gerretsen ECF, Popeijus HE, Annema JT, Clementsen PF, Corbetta L, Gompelmann D, van der Heijden EHFM, Hiddinga BI, van Mook WNKA, Munavvar M, Smeenk FWJM, Groenier M.   +11 more
europepmc   +1 more source

3D Anatomy of the Atrioventricular Conduction Axis Reconstructed Relative to Gross Anatomical Landmarks Using Hierarchical Phase-contrast Tomography. [PDF]

Arrhythm Electrophysiol Rev
Tretter JT, Anderson RH, Ellenbogen KA, Ben-Haim S.   +3 more
europepmc   +1 more source

Spinal Cord Abnormalities in Early Pediatric Multiple Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Spinal cord lesions and atrophy in the cervical region are common in adult multiple sclerosis (MS) and correlate with disability. Whether similar abnormalities occur in pediatric MS patients is largely unknown. Clinical and MRI evaluations were performed in 38 pediatric MS patients and 13 healthy controls (HC).
Monica Margoni, Paola Valsasina, Paolo Preziosa, Martina Rubin, Mor Gueye, Lucia Moiola, Maria Assunta Rocca, Massimo Filippi   +7 more
wiley   +1 more source

Discontinuation of Immunotherapy in Patients With Relapsing Myelitis Without AQP4/MOG Antibodies

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study assesses the outcomes of immunotherapy discontinuation in patients with relapsing seronegative idiopathic myelitis (SIM), a condition that remains uninvestigated due to its rarity. We reviewed records from 77 patients with relapsing SIM at the National Cancer Center of Korea, focusing on 11 who discontinued treatment after a median ...
Ki Hoon Kim, You‐Ri Kang, Jae‐Won Hyun, Su‐Hyun Kim, Ho Jin Kim   +4 more
wiley   +1 more source

Cleft Lip and Palate Digital Impression Workflow. [PDF]

Plast Reconstr Surg Glob Open
Nalabothu P, Benitez BK, de Macedo Santos JW, Mueller AA.   +3 more
europepmc   +1 more source