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=%22Parsopoulou%2C+Faidra%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Parsopoulou%2C+Faidra%22&type=Person&sort=year
Search /vufind/Search2/Results?lookfor=%22Parsopoulou%2C+Faidra%22&type=Person&sort=year
PubPharm (9)
1
Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency
enthalten in:
The journal of allergy and clinical immunology. Global
| 2024
von
Vincent, D.
|
Parsopoulou, F.
|
Martin, L.
| +8
Wird geladen...
2
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)
enthalten in:
Frontiers in allergy
| 2022
von
Parsopoulou, F.
|
Loules, G.
|
Zamanakou, M.
| +13
Wird geladen...
3
SERPING1 Variants and C1-INH Biological Function : A Close Relationship With C1-INH-HAE
enthalten in:
Frontiers in allergy
| 2022
von
Drouet, C.
|
López-Lera, A.
|
Ghannam, A.
| +10
Wird geladen...
4
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor
enthalten in:
Journal of clinical medicine
| 2020
von
Loules, G.
|
Parsopoulou, F.
|
Zamanakou, M.
| +14
Wird geladen...
5
Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients
enthalten in:
Allergy
| 2020
von
Parsopoulou, F.
|
Charignon, D.
|
Tengo, M.
| +6
Wird geladen...
6
A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency
enthalten in:
Allergology international : official journal of the Japanese Society of Allergology
| 2020
von
Vatsiou, S.
|
Zamanakou, M.
|
Loules, G.
| +12
Wird geladen...
7
Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE‐PLG patients
enthalten in:
Allergy
| 2020
von
Parsopoulou, F.
|
Charignon, D.
|
Tengo, M.
| +6
Wird geladen...
8
Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency
enthalten in:
Gene
| 2018
von
Loules, G.
|
Zamanakou, M.
|
Parsopoulou, F.
| +15
Wird geladen...
9
Abstracts from the 10th C1-inhibitor deficiency workshop
enthalten in:
Allergy, asthma and clinical immunology
| 2017
von
Schmaier, A.
|
Cicardi, M.
|
Reshef, A.
| +338
Wird geladen...
1
[1]
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
9
Aufsätze
9
E-Artikel
9
E-Ressourcen
Zeitschriftentitel
2
Allergy
2
Frontiers in allergy
1
Allergology international : official journal of...
1
Allergy, asthma and clinical immunology
1
Gene
1
Journal of clinical medicine
1
The journal of allergy and clinical immunology....
Alle anzeigen ...
weniger ...
Thema
6
Journal Article
3
SERPING1 gene
3
angioedema
2
C1-inhibitor deficiency
2
Complement C1 Inhibitor Protein
2
SERPING1 protein, human
2
next-generation sequencing
1
9001-91-6
1
C1 Inhibitor
1
C1-INH-HAE
1
CPN1 gene
1
Copy number variation
1
Hereditary angioedema
1
Intronic mutations
1
Letter
1
Next-generation sequencing
1
Novel SERPING1 mutations
1
Plasminogen
1
Research Support, Non-U.S. Gov't
1
Review
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
7
2020-
2
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
8
Englisch
Haven't found what you're looking for?
Wird geladen...
