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Gambale, Antonella
38
results:
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1
Complex Modes of Inheritance in Hereditary Red Blood Cell D..:
Andolfo, Immacolata
;
Martone, Stefania
;
Rosato, Barbara Eleni
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304671/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
2
Recommendations for diagnosis and treatment of methemoglobi..:
Iolascon, Achille
;
Bianchi, Paola
;
Andolfo, Immacolata
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291883/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
3
Diagnostic issues faced by a rare disease healthcare networ..:
Limongelli, Giuseppe
;
Iucolano, Stefano
;
Monda, Emanuele
...
info:eu-repo/semantics/altIdentifier/wos/WOS:000764382900001. , 2021
Link:
http://hdl.handle.net/11..
?
4
Apparent recessive inheritance of sideroblastic anemia type..:
Andolfo, Immacolata
;
Martone, Stefania
;
Ribersani, Michela
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716369/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
5
Corrigendum: Characterization of Two Cases of Congenital Dy..:
Russo, Roberta
;
Marra, Roberta
;
Andolfo, Immacolata
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432228/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
6
PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplas..:
Andolfo, Immacolata
;
De Rosa, Gianluca
;
Errichiello, Edoardo
...
info:eu-repo/semantics/altIdentifier/pmid/30930797. , 2019
Link:
http://hdl.handle.net/24..
?
7
Characterization of Two Cases of Congenital Dyserythropoiet..:
Russo, Roberta
;
Marra, Roberta
;
Andolfo, Immacolata
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539198/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
8
Tomographic flow cytometry by digital holography:
Merola, Francesco
;
Memmolo, Pasquale
;
Miccio, Lisa
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062169/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
9
Recommendations regarding splenectomy in hereditary hemolyt..:
Iolascon, Achille
;
Rees, David C
;
de Montalembert, Mariane
...
uri/info:doi/10.3324/haematol.2016.161166. , 2017
Link:
http://hdl.handle.net/20..
?
10
GATA1 erythroid-specific regulation of SEC23B expression an..:
Russo, Roberta
;
Andolfo, Immacolata
;
Gambale, Antonella
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685218/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
11
Recommendations regarding splenectomy in hereditary hemolyt..:
IOLASCON, ACHILLE
;
ANDOLFO, IMMACOLATA
;
Barcellini, Wilma
...
info:eu-repo/semantics/altIdentifier/wos/WOS:000406613200016. , 2017
Link:
http://hdl.handle.net/11..
?
12
New insights on hereditary erythrocyte membrane defects:
Andolfo, Immacolata
;
Russo, Roberta
;
Gambale, Antonella
.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394881/. , 2016
Link:
http://www.ncbi.nlm.nih...
?
13
Functional characterization of novel ABCB6 mutations and th..:
Andolfo, Immacolata
;
Russo, Roberta
;
Manna, Francesco
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967569/. , 2016
Link:
http://www.ncbi.nlm.nih...
?
14
Hypomorphic mutations of SEC23B gene account for mild pheno..:
Russo, Roberta
;
Langella, Concetta
;
Esposito, Maria Rosaria
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3651933. , 2013
Link:
http://www.ncbi.nlm.nih...
?
15
Two founder mutations in the SEC23B gene account for the re..:
Russo, Roberta
;
Gambale, Antonella
;
Esposito, Maria Rosaria
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258542. , 2011
Link:
http://www.ncbi.nlm.nih...
1-15