Results 31 to 40 of about 9,760 (198)

General measures in the treatment of sickle cell disease [PDF]

, 2007
This article presents the most important measures in the care of patients with sickle cell disease, which is characterized by a high morbimortality rate.
Braga, Josefina Aparecida Pellegrini
core   +3 more sources

Natural‐History Mapping of Lysosomal Storage Disorders (LSDs): Gaucher Disease as a Model for Precision Care

Journal of Inherited Metabolic Disease, Volume 49, Issue 1, January 2026.
ABSTRACT Natural‐history datasets have become pivotal for drug development and for shaping clinical‐practice guidelines in rare diseases, yet many lysosomal storage disorders would benefit from deep phenotyping and modern analytic methods. Our objective was to integrate the past decade of genomic, cellular, treatment‐outcome, and regulatory advances ...
Noor Ul Ain, Maya Vaishnaw, Pramod. K. Mistry   +2 more
wiley   +1 more source

The Update, March 22, 2010 [PDF]

, 2010
The Update is a bi-weekly web newsletter published by the Iowa Department of Public Health's Bureau of Family Health. It is posted the second and fourth week of every month, and provides useful job resource information for departmental health care ...

core  

Impact of pneumococcal conjugate vaccination: a retrospective study of hospitalization for pneumonia in North-East Italy [PDF]

, 2016
Introduction. Pneumonia remains a common reason for hospitalizing infants and the elderly worldwide, and streptococcal infection is often responsible. The aim of this study was to assess the burden of pneumonia in a large general population. Methods. All
Baldo, Vincenzo, Baldovin, Tatjana, Bertoncello, Chiara, Buja, Alessandra, Clagnan, E, Cocchio, Silvia, Del Zotto, S, Furlan, Patrizia, Gallo, T, Saia, Mario   +9 more
core   +1 more source

Two Cases of Co-Infection with Babesiosis and Lyme Disease [PDF]

, 2012
Case 1 The patient is a 71-year-old female with past medical history significant for hypothyroidism and hyperlipidemia who presented to Thomas Jefferson University Hospital (TJUH) with complaints of myalgias for 6 weeks duration. The patient stated that
DeCicco, MD, Anthony, Jungkind, PhD, Donald, Kelly, MD, Cecilia, Latreille, MD, Michael, Peiris, MD, B. Niluk   +4 more
core   +2 more sources

Altered translation of GATA1 in Diamond-Blackfan anemia [PDF]

, 2013
Ribosomal protein haploinsufficiency occurs in diverse human diseases including Diamond-Blackfan anemia (DBA)[superscript 1, 2], congenital asplenia[superscript 3] and T cell leukemia[superscript 4].
A Bolze, A Subramanian, Alan H Beggs, BL Ebert, CD Trainor, CG Gkogkas, Colin A Sieff, D Rousseau, DC Dieterich, DG Nathan, DS Peabody, E Kobayashi, E Santini, Eric S Lander, F Gebauer, H Moniz, H Torihara, Hanna T Gazda, Harvey F Lodish, HF Lodish, HT Gazda, HT Gazda, J Cmejlova, J Flygare, J Hu, J Wechsler, Jason R Gotlib, Jennifer C Eng, JJ Welch, JM Lipton, JR Babendure, K Chylicki, K De Keersmaecker, L Garçon, Leif S Ludwig, M Kozak, MJ Weiss, N Kondrashov, NJ Moerke, P Jaako, P Shah, PM Lansdorp, Prathapan Thiru, R Horos, Roxanne Ghazvinian, S Dutt, S Xue, SH Orkin, Stephen W Eichhorn, Tracy I George, V Matys, VG Sankaran, VG Sankaran, VG Sankaran, Vijay G Sankaran   +54 more
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Patients’ with asplenia and doctors’ experiences in implementing preventative measures following a novel educational intervention: a qualitative analysis [PDF]

, 2022
Natascha Anka, Manuela Glattacker, Erik Farin‐Glattacker, Johannes Camp, Siegbert Rieg, Marianne Bayrhuber   +5 more
openalex   +1 more source

European Society for the Study of Coeliac Disease 2025 Updated Guidelines on the Diagnosis and Management of Coeliac Disease in Adults. Part 1: Diagnostic Approach

United European Gastroenterology Journal, Volume 13, Issue 10, Page 1855-1886, December 2025.
Infographic. This infographic summarizes the diagnostic approach to CeD in adults, including initial serological testing, histological confirmation, criteria for a no‐biopsy diagnosis, seronegative CeD, potential CeD, and the role of gluten challenge. Source: Authors' own creation (based on current clinical guidelines).
Abdulbaqi Al‐Toma, Fabiana Zingone, Federica Branchi, Annalisa Schiepatti, Georgia Malamut, Cristina Canova, Isabella Rosato, Honoria Ocagli, Nick Trott, Luca Elli, Alina Popp, Carmen Gianfrani, Renata Auricchio, Andra Neefjes‐Borst, David S. Sanders, Christophe Cellier, Chris J. Mulder, Gerd Bouma, Knut E. A. Lundin, Ludvig M. Sollid, Michael Schumann   +20 more
wiley   +1 more source

Incidental Diagnosis of Situs Inversus Totalis in a 45‐Year‐Old Male Who Presented With Acute Asthma Exacerbation: A Case Report and Brief Literature Review

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Incidental situs inversus totalis (SIT) requires thorough anatomical mapping to exclude associated syndromes (e.g., Kartagener) and congenital anomalies. Early identification, patient education on mirrored anatomy, and multidisciplinary coordination are essential to prevent iatrogenic errors during future interventions, even in asymptomatic ...
Ragasa Getachew Bayisa, Lensa Million Baharu, Mohammed Mecha Abafogi, Yosef Bekele Bonsa, Mohammed Kedir Shukri, Tamirat Godebo Woyimo   +5 more
wiley   +1 more source

The Clinical Presentations of Patients With COVID‐19 in the Omicron Era: Missed Opportunities in the Antiviral Treatment of SARS‐CoV‐2 Infections

Journal of Medical Virology, Volume 97, Issue 10, October 2025.
ABSTRACT COVID‐19 has posed a significant global health challenge. SARS‐CoV‐2 has accumulated several mutations and adapted to humans, with its clinical manifestations evolving from severe bilateral interstitial pneumonia with respiratory failure to predominantly milder forms of disease.
G. Bartolucci, E. Garro, M. Mussa, A. Pepe, R. Angilletta, B. Rizzello, F. A. Ranzani, S. Bonora, G. Di Perri, A. Calcagno   +9 more
wiley   +1 more source