Results 61 to 70 of about 516,925 (316)

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro, Shiwen Koay, Gordon T. Ingle, Patricia McNamara, Laura Watson, Fion Bremner, Valeria Iodice   +6 more
wiley   +1 more source

Idiopathic Orbital Myositis in a Child

, 2013
Idiopathic orbital myositis is seen very rare in children. In this article, the diagnose criteria of a pediatric case with idiopathic orbital myositis and oral non-steroid anti-inflammatory treatment’s response have been evaluated.
Burak Ulaş, Özlem Alkan, Aysel Pelit
core   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

Idiopathic non-familial Acro-osteolysis: A rare case report

Indian Journal of Dermatology, 2012
A 25-year-old woman patient presented with shortening of fingers with racket nails and numerous yellowish papules over the hands and forearms for 21 years. X-ray of the hands revealed destructive osteolytic changes in all the terminal phalanges.
Pijush K Datta, Sanjay Ghosh, Abhishek De   +2 more
doaj   +1 more source

A Two‐Stage Questionnaire and Actigraphy Screening for iRBD in a Multicenter Retrospective Cohort

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Isolated rapid‐eye‐movement sleep behavior disorder is a prodromal marker of synucleinopathies. However, most cases remain undiagnosed due to the insufficient predictive value of questionnaires and limited access to confirmatory video‐polysomnography. We assessed a two‐stage screening strategy combining a brief questionnaire on rapid‐
Caleb A. Massimi, Giorgio Ricciardiello Mejia, Andre Metzger, Kang Hyun Ryu, Salonee Marwaha, Eva Grzegorczyk, Li Zhou, Eliana Jacobs, Boris Gilyadov, Claudia Kunney, Liqhwa Ncube, Ankit Parekh, Emmanuel Mignot, Fanny M. Elahi, Joseph Winer, Kathleen Poston, Andreas Brink‐Kjaer, Emmanuel H. During   +17 more
wiley   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source

Safety of Laparoscopic Splenectomy for Patients with Idiopathic Thrombocytopenic Purpura and Very Low Platelet Count

Caspian Journal of Internal Medicine, 2022
Background: Chronic idiopathic thrombocytopenic purpura (ITP), is an autoimmune disease associated with a reduction in circulating blood platelets under 150x109/L which persists longer than 6 months without any specific cause.
Abbas Abdollahi, Seyed Maryam Naghibi, Hamed Shariat Razavi, Alireza Tavassoli, Azadeh Jabbari Nooghabi, Mehdi Jabbari Nooghabi   +5 more
doaj  

The Costs of a Quiet Disorder: Direct and Indirect Costs of Idiopathic Intracranial Hypertension [PDF]

Idiopathic Intracranial Hypertension (IIH; pseudotumor cerebri) is a disorder with a reported incidence rate of one to three per 100,000 people in the general population.
Brenna Lobb, Daniel Friesner, Robert Rosenman, Emanuel Tanne   +3 more
core  

Double dural spinal sheath:a cadaveric case report [PDF]

, 2010
A previously unreported variation in the anatomy of the spinal dural sheath was observed during routine cadaveric dissection, consisting of a duplication of the dural layer, with layers adherent throughout their length. The double dural sheath completely
Loughenbury, Peter, Soames, Roger, Wadhwani, Sharan   +2 more
core  

Acute Idiopathic Blind Spot Enlargement (AIBSE): Images

, 2023
We present a single case of Acute Idiopathic Blind Spot Enlargement (AIBSE) in a young female patient, including her clinical course and relevant imaging studies.
Andrew R. Osborn, MD; James C. O\u27Brien, MD
core