Results 171 to 180 of about 90,641 (290)

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

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

Unexpected cystoscopic images in a patient with Chronic Granulomatous Disease. [PDF]

Urol Case Rep, 2023
Kowalczyk K, Heropolitańska-Pliszka E.
europepmc   +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

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

Targeted gene editing and near-universal cDNA insertion of CYBA and CYBB as a treatment for chronic granulomatous disease. [PDF]

Nat Commun
Wolff JH, Skov TW, Haslund D, Dorset SR, Revenfeld ALS, Aussel C, Jørgensen SE, Holm M, Thomsen MK, Ammann S, Cathomen T, Mogensen TH, Møller BK, Bak RO, Mikkelsen JG.   +14 more
europepmc   +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

Mold infections in chronic granulomatous disease patients-what comes to the rescue? [PDF]

Bone Marrow Transplant
von Bernuth H, Güngör T.
europepmc   +1 more source

Intestinal microbiome and metabolome signatures in patients with chronic granulomatous disease. [PDF]

J Allergy Clin Immunol, 2023
Chandrasekaran P, Han Y, Zerbe CS, Heller T, DeRavin SS, Kreuzberg SA, Marciano BE, Siu Y, Jones DR, Abraham RS, Stephens MC, Tsou AM, Snapper S, Conlan S, Subramanian P, Quinones M, Grou C, Calderon V, Deming C, Leiding JW, Arnold DE, Logan BR, Griffith LM, Petrovic A, Mousallem TI, Kapoor N, Heimall JR, Barnum JL, Kapadia M, Wright N, Rayes A, Chandra S, Broglie LA, Chellapandian D, Deal CL, Grunebaum E, Lim SS, Mallhi K, Marsh RA, Murguia-Favela L, Parikh S, Touzot F, Cowan MJ, Dvorak CC, Haddad E, Kohn DB, Notarangelo LD, Pai SY, Puck JM, Pulsipher MA, Torgerson TR, Kang EM, Malech HL, Segre JA, Bryant CE, Holland SM, Falcone EL.   +56 more
europepmc   +1 more source

Impaired platelet activation in patients with hereditary deficiency of p47phox [PDF]

, 2018
Azzari, Chiara, Bartimoccia, Simona, Carnevale, Roberto, Loffredo, Lorenzo, Martire, Baldassarre, Nocella, Cristina, Pignata, Claudio, Plebani, Alessandro, Sanguigni, Valerio, Soresina, Annarosa, Violi, Francesco   +10 more
core   +2 more sources