Results 231 to 240 of about 7,512,016 (281)

Umbilical Cord Blood Transplantation Provides an Alternative for Patients With Chronic Granulomatous Disease Lacking HLA-Matched Donors: A PIDTC Report. [PDF]

Transplant Cell Ther
Arnold DE, Leiding JW, Logan B, Marsh RA, Griffith LM, Grunebaum E, Murguía-Favela L, Mallhi K, Chellapandian D, Deal CL, Lim SS, Prasad V, Heimall J, Chandrakasan S, Chen K, Yu LC, Seroogy CM, Gillio A, Bednarski JJ, Kapoor N, Moore TB, Cuvelier GDE, Touzot F, Rayes A, Ebens CL, Schaefer E, Bauchat A, Chopek A, Burroughs L, Cowan MJ, Dvorak CC, Haddad E, Kohn DB, Notarangelo LD, Pai SY, Puck JM, Pulsipher MA, Torgerson T, Malech HL, Kang EM, Parikh S.   +40 more
europepmc   +1 more source

Chronic granulomatous disease: lessons in cell biology from monogenic immunodeficiency. [PDF]

Clin Exp Immunol
Mortimer PM, Svetitsky S, Thomas DC.
europepmc   +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

Gene therapy for X-linked chronic granulomatous disease

Haematologica, 2000

doaj  

Cutaneous Inflammatory Manifestations of Chronic Granulomatous Disease.

JAMA Dermatol
Dev A, Aggarwal R, Vignesh P, Vinay K, Rawat A, Chatterjee D, Dogra S.   +6 more
europepmc   +1 more source

Single-cell and spatial transcriptomics reveal the pathogenesis of chronic granulomatous disease in a natural model

Yu H, Zhang G, Ma Y, Ding J, Liu J, Zhou Z, Jiao S, Dong G, Cai Z.   +8 more
europepmc   +1 more source

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CHRONIC GRANULOMATOUS DISEASE

The Lancet, 1969
Abstract Significant abnormality of nitroblue tetrazolium (N.B.T.) oxidation, and of bacterial killing, in the fathers of patients with chronic granulomatous disease suggests a pattern of sex-modified autosomal recessive inheritance. The data suggest that the defect may be much commoner than is at present recognised.
R K, Chandra, W A, Cope, J F, Soothill
  +7 more sources

Chronic Granulomatous Disease

Pediatric and Developmental Pathology, 2003
CLINICAL SUMMARY A 3-year-old African-American boy presented with limping due to a thigh mass of recent appearance. The lesion was initially painless and nonmobile, without erythema or swelling. There was no fever or other constitutional symptom. Four days before admission, a second tumor appeared on the left parietal region.
Eduardo, Zambrano, Frank, Esper, Rebecca, Rosenberg, Jung, Kim, Miguel, Reyes-Múgica   +4 more
openaire   +4 more sources

Chronic Granulomatous Disease

2023
International ...
Stasia, Marie José, Roos, Dirk
openaire   +2 more sources

Chronic Granulomatous Disease

Pediatric Clinics of North America, 1977
Since 1971, significant deviations from the classic pattern of chronic granulomatous disease have been recognized, and the disease appears to be more common that it did formerly. Knowledge of the basic underlying molecular defect has been broadened, and some new concepts of diagnosis and management have been formed. This report summarizes new knowledge
R B, Johnston, S L, Newman
openaire   +2 more sources