Results 201 to 210 of about 47,697 (254)

Diversification of Aquaculture Production in Relation to Global Change: The Case of the Domestication of Indigenous Euryhaline Catfish Species (Siluriformes) in the Mekong River Delta, Viet Nam

open access: yesReviews in Aquaculture, Volume 18, Issue 1, January 2026.
ABSTRACT The Mekong River Delta, the heart of Vietnam's aquaculture industry, is facing many challenges due to climate change, particularly salinity intrusion. In this context, this review aimed to assess the potential of indigenous euryhaline catfish species to diversify fish farming, strengthen food security, and build resilience in the region. Among
Nguyen Tinh Em   +14 more
wiley   +1 more source

Advanced‐Stage Gonadal Dysgerminoma in a Patient With a Previous Diagnosis of Familial Swyer Syndrome: A Very Rare Genetic Entity

open access: yesCase Reports in Medicine, Volume 2026, Issue 1, 2026.
Introduction Swyer syndrome is a genetic abnormality characterized by a 46,XY karyotype in a phenotypically female individual. Affected individuals typically have average or tall stature, unambiguous genitalia at birth, the presence of Müllerian structures, and bilateral streak gonads.
Süleyman Cemil Oğlak   +10 more
wiley   +1 more source

Severe Hypercalcemia and Confusion in a Middle‐Aged Male: The Hidden Diagnosis of Parathyroid Carcinoma

open access: yesCase Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Parathyroid cancer (PC) is one of the rarest causes of primary hyperparathyroidism (PHPT), typically exhibiting an indolent course but presenting with more severe symptoms compared to its benign counterparts. The diagnosis is most often made postoperatively through histopathological examination; however, certain clinical and biochemical features may ...
Helena Fahmi   +5 more
wiley   +1 more source

StAR Protein Deficiency in Clinical Practice: A Case Series From Saudi Arabia

open access: yesCase Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Objectives Steroidogenic acute regulatory (StAR) protein deficiency is a rare autosomal recessive disorder that disrupts steroid hormone biosynthesis, resulting in congenital adrenal hyperplasia (CAH) and variations in sexual development. However, limited data is available in Saudi Arabia.
Abeer Alabduljabbar   +6 more
wiley   +1 more source

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