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1 . Academic Journal
Temperament and character influence on depression treatment outcome
저자
by
Balestri, Martina
;
Porcelli, Stefano
;
Souery, Daniel
;
Kasper, Siegfried
;
Dikeos, Dimitris
, et al.
소스
In
Journal of Affective Disorders
1 June 2019 252:464-474
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7 . Academic Journal
Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect
저자
by
Sala, Pierguido
;
Colatutto, Antonio
;
Fabbro, Dora
;
Mariuzzi, Laura
;
Marzinotto, Stefania
, et al.
소스
In
European Journal of Medical Genetics
April 2016 59(4):219-222
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7 .
Filamin C (FLNC) truncating mutation in a fatal arrhythmogenic left ventricular cardiomyopathy (ALVC)
저자
by
Simonit, Francesco
;
Da Broi, Ugo
;
D'Elia, Angela Valentina
;
Fabbro, Dora
;
Mio, Catia
, et al.
소스
In
Legal Medicine
July 2024 69
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7 . Academic Journal
Expression of fetal hemoglobin in adult humans exposed to high altitude hypoxia
저자
by
Risso, Angela
;
Fabbro, Dora
;
Damante, Giuseppe
;
Antonutto, Guglielmo
.
소스
In
Blood Cells, Molecules and Diseases
15 March 2012 48(3):147-153
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6 . Academic Journal
Rare spontaneous monochorionic dizygotic twins: a case report and a systematic review.
저자
by
Trombetta, Giulia
;
Fabbro, Dora
;
Demori, Eliana
;
Driul, Lorenza
;
Damante, Giuseppe
, et al.
소스
BMC Pregnancy & Childbirth
. 7/14/2022, Vol. 22 Issue 1, p1-16. 16p.
Open Access (BioMed Central)
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7 . Periodical
A novel de novo NIPA1missense mutation associated to hereditary spastic paraplegia
저자
by
Fabbro, Dora
;
Mio, Catia
;
Fogolari, Federico
;
Damante, Giuseppe
.
소스
Journal of Human Genetics; December 2021, Vol. 66 Issue: 12 p1177-1180, 4p
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6 . Academic Journal
JAK2 V617F-mutated polycythemia vera developing in a patient with a 20-year-long chronic myeloid leukemia at the time of first molecular response
저자
by
Tosoni, Luca
;
Fabbro, Dora
;
Pizzano, Umberto
;
Mullai, Rikard
;
Morelli, Gianluca
, et al.
소스
Annals of Hematology
. 102(5):1279-1280
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7 . Academic Journal
A novel de novo NIPA1 missense mutation associated to hereditary spastic paraplegia
저자
by
Fabbro, Dora
;
Mio, Catia
;
Fogolari, Federico
;
Damante, Giuseppe
.
소스
Journal of Human Genetics
. 66(12):1177-1180
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6 . Academic Journal
NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome.
저자
by
Cavaliere, Elena
;
Gortan, Anna Jolanda
;
Passon, Nadia
;
Fabbro, Dora
;
Marin, Dario
, et al.
소스
Clinical Genetics
. Jul2021, Vol. 100 Issue 1, p114-116. 3p.
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7 . Academic Journal
Fludarabine-based induction therapy does not overcome the negative effect of ABCG2 (BCRP) over-expression in adult acute myeloid leukemia patients
저자
by
Damiani, Daniela
;
Tiribelli, Mario
;
Michelutti, Angela
;
Geromin, Antonella
;
Cavallin, Margherita
, et al.
소스
In
Leukemia Research
2010 34(7):942-945
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