Results 191 to 200 of about 92,991 (335)

A Fatal Case of Chronic Granulomatous Disease in a Young Man. [PDF]

Cureus, 2023
Ho NHH, Patel S, Pathak P.
europepmc   +1 more source

Cutaneous non‐tuberculous mycobacterial infections: A retrospective study of 94 cases from Germany

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background Cutaneous non‐tuberculous mycobacterial infections (NTM) remain a diagnostic and therapeutic challenge. The aim of this study was to characterize cutaneous NTM infections in Germany over a 24‐year‐period. Patients and Methods 73 patients with cutaneous NTM infections diagnosed at 17 different German University Hospitals from 2000 ...
Luisa Bopp, Nicolai Deresz, Henning Klapproth, Isabelle Suárez, Jonathan Jantsch, Mario Fabri, Esther von Stebut   +6 more
wiley   +1 more source

Clinical manifestations of 42 Moroccan patients with chronic granulomatous disease. [PDF]

Qatar Med J
Dably A, Benhssaein I, El Bakkouri J, Drissi Bourhanbour A, Jeddane L, Aziz Bousfiha A, Ailal F.   +6 more
europepmc   +1 more source

Report of 2 Cases of Chronic Granulomatous Disease in Adults

, 2007
Mahdi Eskandarlou, Hashemi Seyed Hamid, M Hajilouei, Azizallah Dehghan, Saba Mohammad Sadegh, H Shahnazari   +5 more
openalex   +1 more source

Chronic granulomatous Herpes simplex encephalitis in a child with DiGeorge syndrome- Expanding the spectrum of Herpes-associated neurological disease [PDF]

Deepti Kewalramani, Yathwin Kanagavel, Visvanathan Krishnaswamy, Latha Ravichandran, Luis de la Cruz‐Merino, Padmasani Venkat Ramanan, Ram Mohan, Ranjith Kumar Manokaran   +7 more
openalex   +1 more source

Chronic granulomatous disease [PDF]

, 2020
INSERM
openalex   +1 more source

Wells syndrome: clinical findings and management in a large cohort of 48 patients

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives: Wells syndrome (WS) is a rare inflammatory skin disorder typically characterized by erythematous, edematous, and pruritic plaques. Despite its distinct histopathological features, WS remains an underdiagnosed disease due to its variable clinical presentations and overlap with other dermatological conditions.
Marco Adriano Chessa, Silvia Robuffo, Tullio Brunetti, Luca Rapparini, Bianca Maria Piraccini, Cosimo Misciali, Beatrice Raone, Iria Neri, Federica Filippi   +8 more
wiley   +1 more source

Interferon-gamma 1b-induced gene expression alters neutrophil function in patients with chronic granulomatous disease. [PDF]

PLoS One
Ambruso DR, Briones NJ, Tran AD, Sanford B, Childs C, Katz BZ, Ellison M, Johnston RB, Jones KL.   +8 more
europepmc   +1 more source

An additional Nsil RFLP at the X-linked chronic granulomatous disease (CYBB) locus [PDF]

, 1990
A Pelham, S Malcolm, R J Levinsky, Christine Kinnon   +3 more
openalex   +1 more source

Oral mucosal manifestations with identical mutations to the bone marrow in a patient with VEXAS syndrome

Rheumatology &Autoimmunity, EarlyView.
Lilian Vasaitis, Lena Blomstrand, Tatjana Pandzic, Miklos Gulyas, Panagiotis Baliakas, Viktor Ljungström   +5 more
wiley   +1 more source