Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Leonilde Pagano"'
Autor:
Leonilde Pagano, Assunta Viola, Gennaro Fioretti, Massimiliano Ammirabile, Paolo Ricchi, Luciano Prossomariti
Publikováno v:
Haematologica, Vol 92, Iss 7 (2007)
Between January 1995 and December 2005, we conducted a screening program for the presence of Hb Neapolis, a rare abnormal Hb variant, in Campania, a region in Southern Italy. Nineteen patients with Hb Neapolis in heterozygosis and six patients with a
Externí odkaz:
https://doaj.org/article/3b801190546e4ef9b8833ec30d8d7097
Autor:
Aldo Filosa, Silvia Costantini, Tiziana Di Matola, Patrizia Cinque, Leonilde Pagano, Anna Spasiano, Caterina Saporito, Massimiliano Ammirabile, Paolo Ricchi
Publikováno v:
Hematology (Amsterdam, Netherlands). 22(7)
To date in Italy, there is paucity on data about the prevalence, clinical and haematological features of patients carrying the haemoglobin (Hb) Lepore variant in homozygous or in association with other haemoglobinopathies.Here we report the results o
Autor:
Giovan Giuseppe Di Costanzo, Luciano Prossomariti, Alfonso Galeota Lanza, Anna Spasiano, Silvia Costantini, Paolo Ricchi, Patrizia Cinque, Tiziana Di Matola, Massimiliano Ammirabile, Leonilde Pagano
Publikováno v:
British Journal of Haematology. 155:524-527
Autor:
S Cutillo, Leonilde Pagano, Emanuele Miraglia del Giudice, Silverio Perrotta, Giovanni Colonna, Filomena de Angelis, Achille Iolascon
Publikováno v:
British Journal of Haematology. 89:933-936
We describe a white Italian kindred in which hereditary elliptocytosis (HE) is associated with abnormal level of alpha I/78 peptide in spectrin digest. Clinical phenotype varied among the family members ranging from asymptomatic to mild haemolytic HE
Autor:
Luciano Prossomariti, Leonilde Pagano, Maria Rosaria D'Amico, Assunta Viola, Felicetto Ferrara, Rossella D'Elia, Daniela Laudati, Massimiliano Ammirabile, Salvatore Palmieri
Publikováno v:
Leukemia & Lymphoma. 47:2331-2334
An increased incidence of HFE gene mutations has been described in hematologic malignancies. In the present study, we investigated the allelic frequency of HFE gene mutations in 154 adult patients with acute leukemia (AL) [107 acute myeloid leukemia
Autor:
Leonilde Pagano, Rossana D'Avino, Clementina Carestia, Maria De Angioletti, Mario Alessi, Laura Manca, G. Lacerra
Publikováno v:
British Journal of Haematology. 126:743-749
A clinical, haematological, biochemical and molecular study was carried out in 17 patients affected with thalassaemia intermedia, who were compound heterozygotes for the beta-thalassaemia mutation beta-87 C-->G to determine the genetic basis of their
Autor:
Mirella Fiorito, Carmelo Magnano, Giovanni Li Volti, Emilia Medulla, Clementina Caresti, Leonilde Pagano, Giuseppina Lacerra, R. Testa
Publikováno v:
Hemoglobin. 26:59-66
Hb G-San Jose or beta7(A4)Glu-->Gly has been reported in Southern Italian or Mexican families. We have studied four families from Sicily and Campania, Southern Italy. In six carriers, the hemoglobin variant level ranged from 32 to 38%. In four double
Publikováno v:
Hemoglobin 25 (2001): 67–78. doi:10.1081/HEM-100103071
info:cnr-pdr/source/autori:V. Carbone; A.M. Salzano; L. Pagano; S. Buffardi; C. De Rosa; P. Pucci/titolo:Identification of Hb Villejuif [Beta 123 (H1) Thr->Ile] in Southern Italy/doi:10.1081%2FHEM-100103071/rivista:Hemoglobin/anno:2001/pagina_da:67/pagina_a:78/intervallo_pagine:67–78/volume:25
info:cnr-pdr/source/autori:V. Carbone; A.M. Salzano; L. Pagano; S. Buffardi; C. De Rosa; P. Pucci/titolo:Identification of Hb Villejuif [Beta 123 (H1) Thr->Ile] in Southern Italy/doi:10.1081%2FHEM-100103071/rivista:Hemoglobin/anno:2001/pagina_da:67/pagina_a:78/intervallo_pagine:67–78/volume:25
Hb Villejuif [beta123(H1)Thr--Ile] is a silent and asymptomatic variant described in 1989 in an 87-year-old woman of French origin suffering from coincidental polycythemia vera. This paper reports the second observation of Hb Villejuif in three relat
Autor:
Leonilde Pagano, Gennaro Musollino, Paola Primignani, Gabriella Mastrolonardo, Romeo Prezioso, Clementina Carestia, Giuseppina Lacerra
Publikováno v:
Annals of hematology. 91(11)
We report a new β-thalassaemia allele detected in a young Italian woman, suffering with mild non-haemolytic anaemia (Hb < 10 g/dL) and not showing Hb variant or Heinz bodies. The allele is characterised by duplication of tetranucleotide ‘AG/CT’
Autor:
Paolo, Ricchi, Alfonso G, Lanza, Massimiliano, Ammirabile, Silvia, Costantini, Patrizia, Cinque, Anna, Spasiano, Tiziana, Di Matola, Giovan G, Di Costanzo, Leonilde, Pagano, Luciano, Prossomariti
Publikováno v:
British journal of haematology. 155(4)