Results 51 to 60 of about 1,914,079 (156)

Melanoma and Other Melanistic Lesions in Brown Bullhead Ameiurus nebulosus From Waterbodies in the Northeastern United States and Canada: Identification of Risk Factors

Journal of Fish Diseases, Volume 49, Issue 11, November 2026.
ABSTRACT Melanistic lesions, including non‐raised black areas due to proliferations of melanocytes and melanomacrophages in the dermis and epidermis, as well as raised black areas consistent with melanoma, are described in brown bullhead (BBH) Ameiurus nebulosus from three water bodies in the northeastern United States and Quebec, Canada.
Vicki S. Blazer, Peter Emerson, Matthew Bodnar, Thomas Jones, David R. Russell, Matthew Pehrson, Cheyenne R. Smith, Danielle Cleveland, Mark J. Henderson, Patricia M. Mazik   +9 more
wiley   +1 more source

[18F]Fluorodeprenyl‐D2 PET as a Tool to Monitor Disease Activity in GAD65‐Ab Autoimmune Encephalitis

Annals of Clinical and Translational Neurology, Volume 13, Issue 10, Page 1978-1992, October 2026.
ABSTRACT Objective To evaluate [18F]fluorodeprenyl‐D2 ([18F]F‐DED) positron‐emission tomography (PET) imaging as a biomarker of disease activity in autoimmune encephalitis (AIE) associated with glutamic acid decarboxylase 65 (GAD65) antibodies. Methods [18F]F‐DED PET was performed in 25 GAD65‐AIE patients and 8 controls using dynamic (0–60 min) and ...
Julia S. Dorneich, Jonathan A. Gernert, Hanna Zimmermann, Lisa Tagnin, Marianthi Zeinaki, Laura Sanzo, Letizia Vogler, Elisabeth Kaufmann, Justina Dargvainiene, Frank Leypoldt, Gérard N. Bischof, Robert Perneczky, Boris‐Stephan Rauchmann, Simon Lindner, Günter U. Höglinger, Rudolf A. Werner, Martin Kerschensteiner, Tania Kümpfel, Matthias Brendel, Franziska S. Thaler   +19 more
wiley   +1 more source

Proteomic Signatures of Noise‐Induced Hearing Loss in the Mouse Cochlea

Cell Biology International, Volume 50, Issue 10, October 2026.
ABSTRACT Hearing loss affects over 1.5 billion people worldwide and has substantial social, educational, and economic consequences. Although genetic studies have identified numerous hearing‐loss‐associated genes, the molecular changes accompanying noise‐induced hearing loss (NIHL) remain incompletely understood.
Ana Carla Batissoco, Danillo Alencar‐Coutinho, Ana Carolina Ferreira‐Scatone, Stella Diogo‐Cavassana, Jeanne Oiticica, Karina Lezirovitz, Ricardo Ferreira Bento   +6 more
wiley   +1 more source

Case description: Prenatal sonographic features of Silver-Russell Syndrome

, 2023
20.500.12530/87857Introduction: Silver-Russell syndrome is a congenital disorder that causes prenatal and postnatal growth restriction, relative macrocephaly, prominent forehead, triangular facies, clinodactyly, body asymmetry, severe feeding ...
Rikeros, E. K., Alvarado, E. Antolin, Santos, L. M. Martin   +2 more
core   +1 more source

Report and review of described associations of Mayer-Rokitansky-Küster-Hauser syndrome and Silver-Russell syndrome

, 2015
Silver–Russell syndrome (SRS) and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome are described in isolation. However, their co-occurrence has only been rarely reported.
Baynam, Gareth S., Deborah JG Mackay, Glynis Price, Karen Carpenter, Mary B Abraham, Abraham, Mary B., Mackay, Deborah J.G., Choong, Catherine S., Gareth S Baynam, Carpenter, Karen, Price, Glynis, Catherine S Choong   +11 more
core   +2 more sources

Russell–Silver Syndrome – A Case Report from Iraq

Mustansiriya Medical Journal
Russell–Silver syndrome (RSS) is an uncommon but clinically important genetic disorder defined by specific dysmorphic features such as relative macrocephaly at birth, body asymmetry, intrauterine growth restriction, and postnatal growth failure.
Wasnaa Hadi Abdullah, Rihab Faisal Alabedi, Mushriq Abdullah Hussein   +2 more
doaj   +1 more source

Plag1 Regulates Sensorimotor Modulation in Zebrafish

International Journal of Developmental Neuroscience, Volume 86, Issue 6, October 2026.
PLAG1 regulates early neurobehavioural development in zebrafish. Reducing plag1 alters craniofacial patterning, increases thigmotaxis and changes responses to light and acoustic stimuli, while gross brain structure and motor neuron development remain largely intact.
Jemma G. Gasperoni, Jarrad N. Fuller, April L. Lewis, Travis K. Johnson, Bert De Groef, Sebastian Dworkin   +5 more
wiley   +1 more source

New clinical and molecular insights into Silver–Russell syndrome

, 2016
International audienceThe purpose of review is to summarize new outcomes for the clinical characterization, molecular strategies, and therapeutic management of Silver-Russell syndrome (SRS)
Giabicani, Eloïse, Netchine, Irène, Brioude, Frédéric   +2 more
core   +1 more source

Silver-Russell syndrome. Clinical and etiopathological aspects of a model genomic imprinting entity [PDF]

, 2020
Silver-Russell syndrome is characterized by asymmetrical intrauterine growth retardation, with normal head circumference and small, pointed chin, which results in a triangular face. It can also include body asymmetry, among other characteristics.
Stock F., Callea M., Zambito V., Cammarata-Scalisi F., Riccio A., Sparago A.   +5 more
core   +1 more source

Challenges in Diagnosing Central Adrenal Insufficiency in Children: Cortisol‐Stimulating Tests are Safe and Often Required

Clinical Endocrinology, Volume 105, Issue 4, Page 408-415, October 2026.
ABSTRACT Introduction The accuracy and safety of cortisol‐stimulating tests (CSTs) for assessing hypothalamic–pituitary–adrenal (HPA) axis integrity, including the diagnosis of central adrenal insufficiency (CAI), in children remain uncertain. Although these tests can simultaneously evaluate cortisol and growth hormone secretion, the present study ...
Mariana Peduti Halah, Ana Carolina Maia Teodózio, Davi Casale Aragon, Paula Conde Lamparelli Elias, Margaret de Castro, Ayrton Custodio Moreira, Sonir Rauber Antonini   +6 more
wiley   +1 more source