Dean R Campagna
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Explore the profile of Dean R Campagna including associated specialties, affiliations and a list of published articles.
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43
Citations
2301
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Recent Articles
1.
Jiang D, Sampino E, Rosenlind K, Campagna D, DiTroia S, Fleming M, et al.
Am J Hematol
. 2025 Mar;
PMID: 40052222
No abstract available.
2.
Ducamp S, Campagna D, Sendamarai A, Schmidt P, Tsai H, Heeney M, et al.
Blood
. 2025 Feb;
PMID: 39912603
X-linked sideroblastic anemia (XLSA) in carrier females of ALAS2 mutations is not uncommon. We describe unique features and genotype/phenotype correlations in XLSA females and evaluate the contributions of X-chromosome skewing...
3.
Stenton S, Laricchia K, Lake N, Chaluvadi S, Ganesh V, DiTroia S, et al.
medRxiv
. 2025 Jan;
PMID: 39763565
Background: Variants in the mitochondrial genome (mtDNA) cause a diverse collection of mitochondrial diseases and have extensive phenotypic overlap with Mendelian diseases encoded on the nuclear genome. The mtDNA is...
4.
Ducamp S, Sendamarai A, Campagna D, Chin D, Fujiwara Y, Schmidt P, et al.
Blood
. 2024 Jun;
144(13):1418-1432.
PMID: 38900972
X-linked sideroblastic anemia (XLSA) and X-linked protoporphyria (XLPP) are uncommon diseases caused by loss-of-function and gain-of-function mutations, respectively, in the erythroid form of 5-aminolevulinic acid synthetase (ALAS), ALAS2, which encodes...
5.
Renella R, Gagne K, Beauchamp E, Fogel J, Perlov A, Sola M, et al.
Am J Hematol
. 2021 Oct;
97(1):18-29.
PMID: 34677878
Septins play key roles in mammalian cell division and cytokinesis but have not previously been implicated in a germline human disorder. A male infant with severe neutropenia and progressive dysmyelopoiesis...
6.
Oakley J, Campagna D, Sun L, Rockowitz S, Sliz P, Boudreaux J, et al.
Pediatr Blood Cancer
. 2021 Aug;
69(1):e29309.
PMID: 34411431
No abstract available.
7.
Heeney M, Berhe S, Campagna D, Oved J, Kurre P, Shaw P, et al.
Hum Mutat
. 2021 Jul;
42(11):1367-1383.
PMID: 34298585
The congenital sideroblastic anemias (CSAs) are a heterogeneous group of inherited disorders of erythropoiesis characterized by pathologic deposits of iron in the mitochondria of developing erythroblasts. Mutations in the mitochondrial...
8.
Frost J, Tan T, Abbas M, Wideman S, Bonadonna M, Stoffel N, et al.
Med
. 2021 Mar;
2(2):164-179.e12.
PMID: 33665641
Background: How specific nutrients influence adaptive immunity is of broad interest. Iron deficiency is the most common micronutrient deficiency worldwide and imparts a significant burden of global disease; however, its...
9.
Crispin A, Guo C, Chen C, Campagna D, Schmidt P, Lichtenstein D, et al.
J Clin Invest
. 2020 Jul;
130(10):5245-5256.
PMID: 32634119
The congenital sideroblastic anemias (CSAs) can be caused by primary defects in mitochondrial iron-sulfur (Fe-S) cluster biogenesis. HSCB (heat shock cognate B), which encodes a mitochondrial cochaperone, also known as...
10.
Yin S, Gambe R, Sun J, Martinez A, Cartun Z, Regis F, et al.
Cancer Cell
. 2019 Feb;
35(2):283-296.e5.
PMID: 30712845
SF3B1 is recurrently mutated in chronic lymphocytic leukemia (CLL), but its role in the pathogenesis of CLL remains elusive. Here, we show that conditional expression of Sf3b1-K700E mutation in mouse...