Results 11 to 20 of about 1,670 (89)

Faunistic inventory of the genus Culicoides (Diptera: Ceratopogonidae) in Mauritius Island, Indian Ocean: Diversity and spatial distribution of species of veterinary interest. [PDF]

Med Vet Entomol
Four Afrotropical Culicoides species are recorded in Mauritius with suspected or historically involvement in BTV and EHDV transmission. All species were distributed all over the island. While intra‐specific morphological variations were detected, genetic analyses did not reveal any cryptic diversity. Abstract Viruses transmitted by biting midge species
Iyaloo DP, Elahee KB, Mosawa VR, Munglee NR, Mahadeo I, Genevieve C, Bhoobun H, Ribon-Chaudat L, Lardeux R, Hammami P, Huber K, Bru D, Grimaud Y, Rasamoelina-Andriamanivo H, Baldet T, Garros C.   +15 more
europepmc   +2 more sources

Epidemiology and economic burden of Wilson disease in France: A nationwide population-based study. [PDF]

J Inherit Metab Dis
Abstract Wilson disease (WD) is a rare inherited copper metabolism disorder characterized by progressive pathological deposition of copper, primarily in the liver and brain. This longitudinal retrospective study conducted using the French national claims (Système National des Données de Santé [SNDS]) database assessed WD prevalence in France, described
Fang S, Furegato M, Azzi J, Couchonnal-Bedoya E, Debray D.   +4 more
europepmc   +2 more sources

ROLUL PROTEINEI ATP7B ÎN HOMEOSTAZIA CUPRULUI ȘI ÎN DEZVOLTAREA BOLII WILSON: REVISTA LITERATURII

Arta Medica, 2022
Obiective. Scopul lucrării prezente constă în studierea funcției proteinei ATP7B la nivel celular și sistemic, implicarea enzimei în menținerea echilibrului intern al ionilor de cupru, precum și rolul ei în dezvoltarea maladiei Wilson.
Veronica Cumpătă
doaj   +1 more source

Lithiases rénales bilatérales et récidivantes révélant une maladie de Wilson

The Pan African Medical Journal, 2015
L'atteinte rénale au cours de la maladie de Wilson est récemment connue. Elle est dominée par l'hypercalciurie souvent asymptomatique et survenant au cours de l'évolution de la maladie.
Salem Bouomrani, Hanéne Nouma, Marwa Neffoussi, Maher Béji   +3 more
doaj   +1 more source

Syndrome parkinsonien secondaire à une maladie de Wilson chez un enfant

The Pan African Medical Journal, 2016
Nous apportons une observation d'un cas de la maladie de Wilson, révélé par un syndrome parkinsonien. Le diagnostic a reposé sur les troubles neuropsychiques, la présence de l'anneau cornéen de Kayser-Fleischer, et les troubles du métabolisme du cuivre ...
Elyajouri Abdelhakim, Abilkacem Rachid, Agadr Aomar   +2 more
doaj   +1 more source

The influence of metaboreflex activation on pulmonary pressure with combined chemoreflex activation in acute and chronic hypoxia

The Journal of Physiology, EarlyView.
Abstract figure legend Activation of both the metaboreflex via post‐exercise circulatory occlusion and the chemoreflex via acute and chronic hypoxia increased pulmonary artery systolic pressure. Coactivation of these reflexes further increased pulmonary artery pressure in an additive manner.
Lauren E. Maier, Elliott J. Jenkins, Andrew Douglas, Jack Talbot, Alexandra Williams, Jonathan Moore, Craig D. Steinback, Liam D. Corr, Zoe H. Adams, Fabio Giuseppe Laginestra, Markus Amann, Philip N. Ainslie, Travis D. Gibbons, Mike Stembridge   +13 more
wiley   +1 more source

Investigator‐Led Research to Improve the Diagnostic Assessment of Platelet Function Disorders: Reflections on the Challenges and Rewards

International Journal of Laboratory Hematology, Volume 48, Issue 4, Page 721-731, August 2026.
ABSTRACT Introduction Investigator‐led research and quality improvement initiatives have led to important improvements in the diagnostic assessment of platelet function disorders (PFD). Methods Personal reflections were used to summarize our contributions to knowledge on PFD diagnostic assessment, pathogenesis, and bleeding risks.
Catherine P. M. Hayward
wiley   +1 more source

Huntington's Disease and Huntington's Disease‐like 2 (HDL2) in Martinique

Movement Disorders Clinical Practice, Volume 13, Issue 3, Page 673-682, March 2026.
ABSTRACT Background Huntington's Disease‐like 2 (HDL2), caused by a CAG repeat expansion in JPH3, closely resembles HD. All reported HDL2 patients to date have some African ancestry. While both disorders exist in the Caribbean, their relative frequency and clinical characteristics remain largely unknown.
Ignacio Antolin‐Sanfeliz, Anna‐Gaelle Giguet‐Valard, Sophie Duclos, Cécile Cazeneuve, Chloé Angelini, Aïssatou Signaté, Russell L. Margolis, Cyril Goizet, Rémi Bellance   +8 more
wiley   +1 more source

The Risk of Transmission of Genetic Prion Diseases is Greater Than 50%

European Journal of Neurology, Volume 32, Issue 12, December 2025.
This study investigated whether transmission ratio distortion (TRD) occurs in inherited prion diseases, specifically familial Creutzfeldt‐Jakob disease (p.E200K variant) and fatal familial insomnia (p.D178N variant), despite the theoretical 50% autosomal dominant inheritance risk.
Izaro Kortazar‐Zubizarreta, Africa Manero‐Azua, Hasier Eraña, Urko Aguire, Joaquín Castilla, Guiomar Perez de Nanclares   +5 more
wiley   +1 more source

Telepathy, Other Minds, and Category Errors

European Journal of Philosophy, Volume 33, Issue 3, Page 1088-1099, September 2025.
Abstract In this paper, I explore several issues surrounding what is called “telepathy” in the context of the problem of other minds. I begin with a quick review of the conditions in which this notion arose and the difficulties to which it gave rise upon its introduction.
Sébastien Motta
wiley   +1 more source