Results 151 to 160 of about 94,325 (274)

Behavioral Phenotype and Neuropsychological Profile of an Adult With Smith‐Magenis Syndrome due to a Previously Unreported RAI1 Mutation: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Smith‐Magenis Syndrome (SMS) is an uncommon genetic disorder caused by microdeletions of chromosome 17p11.2 including the RAI1 gene, or loss‐of‐function mutations that directly affect RAI1. Due to the involvement of RAI1 in neurodevelopment, SMS leads to typical pathologic features in the behavioral and physical phenotype that must be ...
Edgar Andrés Chavarría‐Martínez   +4 more
wiley   +1 more source

Management of Thyroid Eye Disease: A Comparison Between Three Recent Clinical Guidelines. [PDF]

open access: yesOphthalmol Ther
Lei C   +7 more
europepmc   +1 more source

Solid Subtype of Papillary Thyroid Carcinoma: A Case Series Highlighting Aggressive Features

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
Hematoxylin and eosin (H&E) stained section, 40×. Tumor cells with “Orphan Annie eye” nuclei arranged in solid nests. ABSTRACT Papillary thyroid carcinoma (PTC) is the most common malignant thyroid neoplasm. Its solid/trabecular subtype (STPTC) is rare, and its aggressiveness remains controversial.
Rafael Castellanos Bueno   +4 more
wiley   +1 more source

Retinal Microvascular and Orbital Structural Alterations in Thyroid Eye Disease. [PDF]

open access: yesJ Clin Med
Jelušić V   +8 more
europepmc   +1 more source

When Antibiotics Leave a Mark: Minocycline‐Induced Hyperpigmentation

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
Bluish discoloration of the dorsal aspects of the hands and nails. ABSTRACT This article presents two patients with significant minocycline‐induced hyperpigmentation, illustrating the diverse clinical manifestations across various body sites. Judicious use of minocycline and early recognition of its adverse effects are crucial to reduce the risk of ...
Clarissa Ting   +3 more
wiley   +1 more source

Familial Mediterranean fever in northwest of Iran (Ardabil): The first global report from Iran [PDF]

open access: yes
Familial Mediterranean fever (FMF), which is the prototype of the hereditary periodic fever syndromes, is common in the countries around the Mediterranean Sea. Considering its geographical position in the northwest of Iran, with its population of Turkish
امامی, دینا   +10 more
core  

Severe Headache and Acute Blindness: A Case of Pituitary Apoplexy

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Pituitary apoplexy is a rare, life‐threatening syndrome that commonly occurs in the adenomatous pituitary gland. It presents with a myriad of severe neuroendocrine and ophthalmological signs and symptoms. Early diagnosis and prompt treatment are vital in the management of pituitary apoplexy.
Abdul‐Rahman Faiza   +4 more
wiley   +1 more source

Cell migration, chimerism, and graft acceptance [PDF]

open access: yes, 1992
A.J Demetris   +47 more
core   +1 more source

Home - About - Disclaimer - Privacy