Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Tannorella%2C+Pierpaola%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Tannorella%2C+Pierpaola%22&type=Person&sort=year
Search /vufind/Search2/Results?lookfor=%22Tannorella%2C+Pierpaola%22&type=Person&sort=year
PubPharm (36)
1
Prenatal testing for imprinting disorders : A laboratory perspective
enthalten in:
Prenatal diagnosis
| 2023
von
Beygo, J.
|
Russo, S.
|
Tannorella, P.
| +4
Wird geladen...
2
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development
enthalten in:
Cancers
| 2023
von
Luca, M.
|
Carli, D.
|
Cardaropoli, S.
| +19
Wird geladen...
3
Case report : atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum
enthalten in:
Frontiers in genetics
| 2023
von
Vimercati, A.
|
Tannorella, P.
|
Orlandini, E.
| +8
ErratumIn: Front Genet. 2024 Jan 25;15:1372019. - PMID 38333621
Wird geladen...
4
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
Wird geladen...
5
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
Wird geladen...
6
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
Wird geladen...
7
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
Wird geladen...
8
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques
enthalten in:
Clinical genetics
| 2022
von
Carli, D.
|
Operti, M.
|
Russo, S.
| +21
Wird geladen...
9
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny
enthalten in:
Clinical epigenetics
| 2022
von
Tannorella, P.
|
Calzari, L.
|
Daolio, C.
| +8
Wird geladen...
10
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny
enthalten in:
Clinical epigenetics
| 2022
von
Tannorella, P.
|
Calzari, L.
|
Daolio, C.
| +8
Wird geladen...
1
2
3
4
Nächster »
[4]
Filter & Sortierung
Treffer pro Seite
10
20
50
Sortieren
Relevanz
Neueste zuerst
Älteste zuerst
Verfasser
Zeitschriftentitel
Bibliothek
Standort (Printmedien)
Verwandte Substanzen
Verwandte Substanzen werden ermittelt...
Verwandte Erkrankungen/Symptome
Verwandte Erkrankungen/Symptome werden ermittelt...
Verwandte Gene
Verwandte Gene werden ermittelt...
Systematic Reviews
Clinical Studies
Patente
Covid-19/SARS-CoV-2
Exclude Systematic Reviews
Exclude Clinical Studies
Exclude Patents
Medienart
36
Aufsätze
26
E-Artikel
26
E-Ressourcen
10
Gedruckte Aufsätze
Zeitschriftentitel
11
Clinical epigenetics
2
Antioxidants & redox signaling
2
Journal of Alzheimer's disease
2
Journal of Alzheimer's disease : JAD
2
Mechanisms of ageing and development
2
Neuroscience letters
1
American journal of neurodegenerative disease
1
BioMed research international
1
Cancers
1
Clinical Genetics
1
Clinical genetics
1
Epigenomics
1
Frontiers in genetics
1
Genes
1
Human reproduction
1
Human reproduction (Oxford, England)
1
International journal of molecular sciences
1
Journal of clinical medicine
1
Metabolites
1
Mutation research
Alle anzeigen ...
weniger ...
Thema
20
Journal Article
11
Research Support, Non-U.S. Gov't
8
Imprinting disorders
6
Alzheimer’s disease
6
EC 1.5.1.20
6
MTHFR protein, human
6
Methylenetetrahydrofolate Reductase (NADPH2)
5
Beckwith–Wiedemann syndrome spectrum
5
DNA (Cytosine-5-)-Methyltransferases
5
EC 2.1.1.37
5
MTHFR
4
935E97BOY8
4
DNA methylation
4
Differentially methylated regions
4
Epimutations
4
Folic Acid
4
Gain of methylation
4
Genetic testing
4
Growth disturbances
4
Loss of methylation
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
19
2020-
17
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
33
Englisch
Haven't found what you're looking for?
Wird geladen...