Results 51 to 60 of about 361,175 (190)
CNS Neuroscience &Therapeutics, Volume 32, Issue 8, August 2026.CRC‐related neurological disorders are mainly caused by variants in the CHD and BAF complex. The predominant phenotypes of CRC‐related neurological disorders were GDD/ID and epilepsy. Variants in the CHD and BAF complexes have different phenotypes.
Shimeng Chen +9 more
wiley +1 more source
Essential embryology for the Canadian pathologists’ assistant
Anatomical Sciences Education, Volume 19, Issue 7, Page 1134-1156, July 2026.Abstract Pathologists' assistants (PAs) are pivotal in healthcare, conducting autopsies and examining tissues under a pathologist's guidance. Embryology knowledge is crucial for PAs to accurately assess anomalies and identify pathologies. Yet, it is often overlooked in academic PA training programs.
Samantha H. Nacci +4 more
wiley +1 more source
ЕPILEPTIC SEIZURES IN PATIENTS WITH CRANIOVERTEBRAL JUNCION ANOMALY
Эпилепсия и пароксизмальные состояния, 2016 Purpose: Studing seizure in patients with Chiari I malformation. Methods: 111 patients (58 females, 53 males) with Arnold-Chiari I malformation and epilepsy were examined with cognitive and behavioral examinations, EEG, MRI. Results: Patients with Arnold-
M. R. Yarmuchametova
doaj
Clinical Case Reports, 2023 A 6‐year‐old girl with persistent headaches and the visual problem was diagnosed as a delayed onset cranial pansynostosis with concurrent type 1.5 Arnold‐Chiari malformation. She underwent multi‐sutural reconstructive surgery and followed.
Homayoun Tabesh +6 more
doaj +1 more source
Prenatal sonographic evaluation of Arnold Chiari II Malformation [PDF]
, 2017 Arnold Chiari malformations are a broad group of malformations with distinctive imaging findings. They are named after an Austrian pathologist Hans Chiari who first identified types I-III in 1891.
kumar K, Praful +5 more
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Brain and Behavior, Volume 16, Issue 2, February 2026.Comorbidity was present in approximately half of the patients with relapsing‐remitting multiple sclerosis in this Finnish cross‐sectional cohort. Comorbidities, especially psychiatric diseases, were associated with lower persistence on injectable disease‐modifying treatments.
Henrik Ahvenjärvi +4 more
wiley +1 more source
Gitelman and Bartter Syndrome in a Patient With Morbid Obesity: A Case Report and Literature Review
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT We present a case study of a 34‐year‐old man with morbid obesity and a suspected Bartter–Gitelman spectrum tubulopathy (without genetic confirmation), weighing 135 kg, and with a BMI of 42.5 kg/m2, who was referred to the metabolic and bariatric surgery department due to morbid obesity to address abnormal electrolyte levels.
Solmaz Hasani +4 more
wiley +1 more source
The Impact of Syrinx on Clinical Outcomes in Arnold-Chiari Malformation: A Retrospective Study [PDF]
Objective: Arnold-Chiari malformation is congenital or acquired anomaly of the hindbrain that leads to crowding of the cerebellum and brainstem in the posterior cranial fossa.
Mohammad Nasir +3 more
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Arnold-Chiari Malformasyonu [PDF]
, 2022 Arnold-Chiari veya kısaca Chiari malformasyonu; serebellumun tonsillerinin foramen magnum yoluyla aşağıya servikal spinal kanal içerisine hernie olması ile karaktarizedir ve malformasyona intrakranial veya ekstrakranial gelişimsel defektler eşlik ...
Akdemir, Hidayet, Doğu, Hüseyin
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Южно-Российский онкологический журнал, 2023 Today, an Arnold-Chiari malformation is defined as a developmental pathology of the craniovertebral junction manifested by a discrepancy between the volume and contents of the posterior cranial fossa, which in turn leads to compression of neurological ...
E. E. Rostorguev +7 more
doaj +1 more source