Carella M - Search Results

1

Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia.

Rees DC, Iolascon A, Carella M, O'marcaigh AS, Kendra JR, Jowitt SN, Wales JK, Vora A, Makris M, Manning N, Nicolaou A, Fisher J, Mann A, Machin SJ, Clayton PT, Gasparini P, Stewart GW. Rees DC, et al. Among authors: carella m. Br J Haematol. 2005 Jul;130(2):297-309. doi: 10.1111/j.1365-2141.2005.05599.x. Br J Haematol. 2005. PMID: 16029460 Free article.

2

Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).

Iolascon A, Stewart GW, Ajetunmobi JF, Perrotta S, Delaunay J, Carella M, Zelante L, Gasparini P. Iolascon A, et al. Among authors: carella m. Blood. 1999 May 1;93(9):3120-3. Blood. 1999. PMID: 10216110 Free article.

3

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Carella M, Stewart G, Ajetunmobi JF, Perrotta S, Grootenboer S, Tchernia G, Delaunay J, Totaro A, Zelante L, Gasparini P, Iolascon A. Carella M, et al. Am J Hum Genet. 1998 Sep;63(3):810-6. doi: 10.1086/302024. Am J Hum Genet. 1998. PMID: 9718354 Free PMC article.

4

A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.

Carella M, d'Adamo AP, Grootenboer-Mignot S, Vantyghem MC, Esposito L, D'Eustacchio A, Ficarella R, Stewart GW, Gasparini P, Delaunay J, Iolascon A. Carella M, et al. Eur J Hum Genet. 2004 Dec;12(12):1073-6. doi: 10.1038/sj.ejhg.5201280. Eur J Hum Genet. 2004. PMID: 15470366

5

Congenital dyserythropoietic anemia type II in human patients is not due to mutations in the erythroid anion exchanger 1.

Perrotta S, Luzzatto L, Carella M, Iolascon A. Perrotta S, et al. Among authors: carella m. Blood. 2003 Oct 1;102(7):2704-5. doi: 10.1182/blood-2003-07-2389. Blood. 2003. PMID: 14504075 Free article. No abstract available.

6

Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia.

Carella M, Stewart GW, Ajetunmobi JF, Schettini F Jr, Delaunay J, Iolascon A. Carella M, et al. Haematologica. 1999 Sep;84(9):862-3. Haematologica. 1999. PMID: 10477465 No abstract available.

7

Nanotechnologies and microchips in genetic diseases.

Carella M, Volinia S, Gasparini P. Carella M, et al. J Nephrol. 2003 Jul-Aug;16(4):597-602. J Nephrol. 2003. PMID: 14696766 Review.

8

Genetic heterogeneity of congenital dyserythropoietic anemia type II.

Iolascon A, De Mattia D, Perrotta S, Carella M, Gasparini P, Lambertenghi Deliliers G. Iolascon A, et al. Among authors: carella m. Blood. 1998 Oct 1;92(7):2593-4. Blood. 1998. PMID: 9746803 Free article. No abstract available.

9

[Diagnosis of hereditary hemochromatosis with molecular analysis of DNA in patients with anti-HCV positive liver cirrhosis. Clinical case].

Carella AM, Bianco G, Carella M, Gasparini P. Carella AM, et al. Among authors: carella m. Minerva Med. 1998 Sep;89(9):323-7. Minerva Med. 1998. PMID: 9856121 Italian.

10

Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.

Lanzara C, Ficarella R, Totaro A, Chen X, Roberto R, Perrotta S, Lasalandra C, Gasparini P, Iolascon A, Carella M. Lanzara C, et al. Among authors: carella m. Blood Cells Mol Dis. 2003 Jan-Feb;30(1):22-9. doi: 10.1016/s1079-9796(03)00009-3. Blood Cells Mol Dis. 2003. PMID: 12667984

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