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1 . Academic Journal
Null allele can bring to interpretative problems in a deficitary paternity case
저자
by
Di Nunzio, Aldo
;
Tinto, Nadia
;
Iafusco, Fernanda
;
Zibetti, Angelica
;
Ricci, Pietrantonio
, et al.
소스
In
Forensic Science International: Genetics Supplement Series
December 2022 8:115-116
Full Text (ScienceDirect)
Scopus
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7 . Academic Journal
Un caso complesso di attribuzione di paternita'.
저자
by
Di Nunzio, Aldo
;
Di Nunzio, Ciro
;
Maione, Giovanna
;
Iafusco, Fernanda
;
Tinto, Nadia
.
소스
Biochimica Clinica
. Dec2023, Vol. 47 Issue 4, pe56-e61. 4p.
Scopus
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7 . Academic Journal
Can obesity exacerbate hyperinsulinaemia in the presence of the mutation of an insulin receptor gene?
저자
by
Calcaterra, Valeria
;
Zuccotti, Gianvincenzo
;
Mari, Alessandra
;
Iafusco, Fernanda
;
Maione, Giovanna
, et al.
소스
Clinical Obesity
. Dec2023, Vol. 13 Issue 6, p1-5. 5p.
JCR 저널정보
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7 . Academic Journal
An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment.
저자
by
Di Candia, Francesca
;
Di Iorio, Valentina
;
Tinto, Nadia
;
Bonfanti, Riccardo
;
Iovino, Claudio
, et al.
소스
Italian Journal of Pediatrics
. 11/30/2023, Vol. 49 Issue 1, p1-8. 8p.
Open Access (BioMed Central)
Web of Science
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7 . Academic Journal
Combined MITOchondrial-NUCLEAR (MITO-NUCLEAR) Analysis for Mitochondrial Diseases Diagnosis: Validation and Implementation of a One-Step NGS Method.
저자
by
Barretta, Ferdinando
;
Uomo, Fabiana
;
Caldora, Filomena
;
Mocerino, Rossella
;
Adamo, Daniela
, et al.
소스
Genes
. May2023, Vol. 14 Issue 5, p1087. 13p.
Web of Science
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7 . Academic Journal
Analysis of Corneal Deformation in Paediatric Patients Affected by Maturity Onset Diabetes of the Young Type 2.
저자
by
Lanza, Michele
;
Mozzillo, Enza
;
Boccia, Rosa
;
Fedi, Ludovica
;
Di Candia, Francesca
, et al.
소스
Diagnostics (2075-4418)
. Apr2023, Vol. 13 Issue 8, p1500. 10p.
Web of Science
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7 .
Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother
저자
by
Longobardi, Elena
;
Miceli, Francesco
;
Secondo, Agnese
;
Cicatiello, Rita
;
Izzo, Antonella
, et al.
소스
In
Stem Cell Research
May 2021 53
Full Text (ScienceDirect)
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7 . Academic Journal
The Pathogenic Diagnosis in Pediatric Diabetology: Next Generation Sequencing and Precision Therapy.
저자
by
Maione, Giovanna
;
Iafusco, Fernanda
;
Zanfardino, Angela
;
Piscopo, Alessia
;
Ozen, Gulsum
, et al.
소스
Medicina (1010660X); Feb2023, Vol. 59 Issue 2, p310, 7p
Web of Science
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7 . Primary Source
Molecular diagnosis of MODY3 permitted to reveal a de novo 12q24.31 deletion and to explain a complex phenotype in a young diabetic patient
저자
by
Iafusco, Fernanda
;
De Sanctis, Paola
;
Pirozzi, Daniele
;
Capone, Silvana
;
Lombardo, Barbara
, et al.
소스
Clinical Chemistry and Laboratory Medicine (CCLM)
. 57(12):e306-e310
Full Text(De Gruyter)
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7 . Academic Journal
The Association of Autoimmune Diseases with Type 1 Diabetes Mellitus in Children Depends Also by the Length of Partial Clinical Remission Phase (Honeymoon).
저자
by
Ozen, Gulsum
;
Zanfardino, Angela
;
Confetto, Santino
;
Piscopo, Alessia
;
Casaburo, Francesca
, et al.
소스
International Journal of Endocrinology
. 1/4/2020, p1-6. 6p.
Web of Science
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