Results 171 to 180 of about 60,446 (292)

From diagnosis to disease-specific treatment: first experience with enzyme replacement therapy for Fabry disease in North Macedonia-a case series. [PDF]

Front Med (Lausanne)
Karanfilovski V, Nikolov IG, Dzekova Vidimliski P, Balkanov SK, Severova G, Stojanoska A, Gjorgjievski N.   +6 more
europepmc   +1 more source

Exceptional Light Propagation via Generalized Bulk‐Edge Correspondence

Nanophotonics, Volume 15, Issue 13, 13 July 2026.
We show that unlike in electronic systems, localized edge states in topological photonics are governed not only by nontrivial bulk topology, but also by polarization‐dependent light‐line confinement conditions inherent to Maxwell's equations. This fundamentally generalized bulk‐edge correspondence unlocks new regimes of tunable near‐cutoff localization
Heitor da Silva, Sergey K. Ivanov, Isaac Suárez, José R. Salgueiro, Albert Ferrando   +4 more
wiley   +1 more source

A Rare Case of Fabry Disease Combined With Idiopathic Multicentric Castleman Disease and Membranous Nephropathy. [PDF]

Kidney Med
Oka M, Suzuki R, Akasaka T.
europepmc   +1 more source

Fabry disease in Poland [PDF]

Polish Archives of Internal Medicine, 2018
Bazan-Socha, Stanisława, Kuczia, Paweł, Musiał, Jacek, Błażejewska-Hyżorek, Beata   +3 more
openaire   +4 more sources

Photonic Doping of Epsilon‐Near‐Zero Bragg Microcavities

Nanophotonics, Volume 15, Issue 13, 13 July 2026.
Photonic doping of an epsilon‐near‐zero (ENZ) Bragg microcavity at optical frequencies induces strong magnetic responses from dielectric inclusions, enabling intense field localization, Purcell enhancement, and tunable hybrid Bragg–Mie modes. The platform supports perfect magnetic conductor and epsilon‐and‐mu‐near‐zero regimes, offering opportunities ...
Ali Panahpour, Jussi Kelavuori, Mikko Huttunen   +2 more
wiley   +1 more source

Newborn screening for Fabry disease in Japan: an additional 3-year report. [PDF]

Mol Genet Metab Rep
Sawada T, Kido J, Sugawara K, Yoshida S, Inoue T, Hirose S, Nakamura K.   +6 more
europepmc   +1 more source

Fabry disease: Enfermedad de fabry

, 2018
RESUMEN La enfermedad de Fabry es una enfermedad de depósito lisosomal causada por la deficiencia de la enzima alfa galactosidasa A, con patrón de herencia ligado al cromosoma X. El cuadro clínico tiene una variedad de síntomas y signos; y se han descrito una variante clínica clásica y variantes clínica no clásica como la renal o cardíaca.
openaire   +1 more source

Could Fabry Disease Cause Giant Coronary Aneurysms in a 7‐Month‐Old Infant: A Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Fabry disease is a rare X‐linked lysosomal storage disorder that can affect multiple organs. Cardiac involvement, one of its significant manifestations, can begin in childhood and is more prevalent in males, with severity increasing with age and disease progression.
Reza Shabanian, Minoo Dadkhah, Rana Doroudian, Mehrnaz Adib, Sahar Naderi, Khashayar Ashkboos   +5 more
wiley   +1 more source

Persistent Hematuria and Proteinuria in a Patient with SLE Nephritis. [PDF]

Kidney360
Singh T, Panzer SE, Garg S.
europepmc   +1 more source

Psychometric Properties of the Commitment to Exercise Scale in Inpatients With Anorexia Nervosa and Bulimia Nervosa

European Eating Disorders Review, Volume 34, Issue 4, Page 1121-1129, July 2026.
ABSTRACT Objective Compulsive exercise is a common behaviour among persons with eating disorders, particularly in those with anorexia nervosa (AN) and bulimia nervosa (BN). In the current study, we examined psychometric properties of a German version of the eight‐item Commitment to Exercise Scale (CES) with a four‐point scale response format.
Fiona M. Fabry, Sandra Schlegl, Nina Dittmer, Ulrich Voderholzer, David R. Kolar, Adrian Meule   +5 more
wiley   +1 more source