Results 141 to 150 of about 60,964 (282)

Results of a prospective observational study of imiglucerase biosimilar in adults with type I Gaucher disease

Терапевтический архив
Aim. To collect and analyze real-world data on long-term enzyme replacement therapy with Glurazyme® in patients with type I Gaucher disease (GD). Materials and methods.
Elena A. Lukina, Rodion V. Ponomarev, Galina N. Salogub, Vadim A. Bezrukikh, Elena V. Saifullina, Igor L. Davydkin, Svetlana A. Volkova, Tatiana V. Shelekhova, Marina V. Kosinova, Evgeniy V. Vasiliev, Elena G. Kirillova, Olesya E. Danilova, Rais K. Khairetdinov, Oksana A. Markova, Evgene V. Zuev, Anton I. Borozinets   +15 more
doaj   +1 more source

Severe vitamin B12 deficiency with pancytopenia, hepatosplenomegaly and leukoerythroblastosis in two Syrian refugee infants: a challenge to differentiate from acute leukaemia

BMJ Case Reports, 2014
B. Belen, B. Hismi, U. Koçak
semanticscholar   +1 more source

Clinical Patterns of Osteoarticular, Bone Marrow and Urogenital Paracoccidioidomycosis

Mycoses, Volume 69, Issue 5, May 2026.
ABSTRACT Background Paracoccidioidomycosis (PCM) is an endemic systemic mycosis in Latin America, classically characterized by pulmonary, mucosal and lymphatic involvement. Extrapulmonary manifestations affecting uncommon organs remain poorly characterized and may contribute to diagnostic delay and adverse outcomes. Methods We conducted a retrospective
Wdson Luis Lima Kruschewsky, Mariane Cappellini Stricagnolo, Mônica Scarpelli Martinelli Vidal, Gil Benard, Vítor Falcão de Oliveira, Tiago Alexandre Cocio, Adriana Satie Gonçalves Kono Magri, Marcello Mihailenko Chaves Magri   +7 more
wiley   +1 more source

Hemophagocytic lymphohistiocytosis following enteric fever: A rare autopsy case report

Indian Journal of Pathology and Microbiology
Hemophagocytic lymphohistiocytosis (HLH) is a severe and frequently underdiagnosed disorder of systemic immune dysregulation resulting in hypercytokinemia and histologically evident hemophagocytosis, We report a case of a 34-year-old man who presented ...
Gwendolyn Fernandes, Pooja Mhashete, Pranav Pramod Patwardhan   +2 more
doaj   +1 more source

Hepatosplenomegaly [PDF]

Proceedings of the Royal Society of Medicine, 1947
J. P. M. Tizard, Donald Paterson
openaire   +1 more source

Facial hypertrichosis, hyperpigmentation, and hepatosplenomegaly [PDF]

European Journal of Internal Medicine, 2021
Paola E. Pizano, Edwin Uriel Suárez
openaire   +2 more sources

A Fatal Case of Generalized Lysosomal Storage Disease in an Infant. [PDF]

, 2010
Gangliosidoses are a heterogeneous group of lysosomal storage diseases with an autosomal recessive trait, which are characterized by the intracellular accumulation of gangliosides in several tissues, mainly in neurons.
Ancer Rodríguez, Jesús, Barboza Quintana, Oralia, Barboza Quintana, Álvaro, Garza Alatorre, Arturo Gerardo, Melo de la Garza, Américo, Ponce Camacho, Marco Antonio, Ramírez Bon, Enrique, Rodríguez Gutiérrez, Nora Alicia   +7 more
core  

Hemophagocytic Lymphohistiocytosis Syndrome Associated with Gaucher Disease Type 2

Turkish Journal of Hematology, 2014
Gholamreza Bahoush, Ghasem Miri Aliabad
doaj   +1 more source

Elevated serum aminotransferases in an infant with failure to thrive: A clinicopathological case report

JPGN Reports, Volume 7, Issue 2, Page 340-348, May 2026.
Jamie M. Klapp, Lauren Nichols, Nicholas J. Gloude, Amber Hildreth, Kathleen B. Schwarz   +4 more
wiley   +1 more source

Hepatosplenomegaly

Paediatrics and Child Health, 2017
openaire   +2 more sources