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/vufind/Search/Results?lookfor=%22Girardi%2C+Katia%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Girardi%2C+Katia%22&type=Person&sort=year
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PubPharm (26)
1
The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman-like lymphadenopathies : A 20-year retrospective analysis of clinical and pathological features
enthalten in:
British journal of haematology
| 2024
von
Pelliccia, S.
|
Rogges, E.
|
Cardoni, A.
| +18
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2
The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman‐like lymphadenopathies : A 20‐year retrospective analysis of clinical and pathological features
enthalten in:
British Journal of Haematology
| 2024
von
Pelliccia, S.
|
Rogges, E.
|
Cardoni, A.
| +18
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3
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype-phenotype Association
enthalten in:
Journal of clinical immunology
| 2023
von
Roncareggi, S.
|
Girardi, K.
|
Fioredda, F.
| +25
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4
Germline bi-allelic SH2B3/LNK alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorder
enthalten in:
Haematologica
| 2023
von
Arfeuille, C.
|
Vial, Y.
|
Cadenet, M.
| +22
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5
Impact of Mercaptopurine Metabolites on Disease Outcome in the AIEOP-BFM ALL 2009 Protocol for Acute Lymphoblastic Leukemia
enthalten in:
Clinical pharmacology and therapeutics
| 2023
von
Franca, R.
|
Stocco, G.
|
Kiren, V.
| +14
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6
A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association
enthalten in:
Journal of clinical immunology
| 2023
von
Roncareggi, S.
|
Girardi, K.
|
Fioredda, F.
| +25
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7
GAU-PED study for early diagnosis of Gaucher disease in children with splenomegaly and cytopenia
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Pession, A.
|
Di Rocco, M.
|
Venturelli, F.
| +28
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8
GAU-PED study for early diagnosis of Gaucher disease in children with splenomegaly and cytopenia
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Pession, A.
|
Di Rocco, M.
|
Venturelli, F.
| +17
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9
GAU-PED study for early diagnosis of Gaucher disease in children with splenomegaly and cytopenia
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Pession, A.
|
Di Rocco, M.
|
Venturelli, F.
| +17
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10
Paraneoplastic pemphigus and Castleman's disease : a case report and a revision of the literature
enthalten in:
Italian journal of pediatrics
| 2023
von
Irrera, M.
|
Bozzola, E.
|
Cardoni, A.
| +6
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Medienart
26
Aufsätze
24
E-Artikel
24
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2
Gedruckte Aufsätze
Zeitschriftentitel
6
British journal of haematology
3
Cancers
3
Orphanet journal of rare diseases
2
British Journal of Haematology
2
Haematologica
2
Journal of clinical immunology
1
Blood advances
1
Clinical Pharmacology & Therapeutics
1
Clinical pharmacology and therapeutics
1
International journal of molecular sciences
1
Italian journal of pediatrics
1
Medical mycology
1
Pediatric blood & cancer
1
The Italian journal of pediatrics
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Thema
16
Journal Article
5
Research Support, Non-U.S. Gov't
4
Review
3
Cytopenia
3
Gaucher disease
3
Lysosomal storage disease
3
Splenomegaly
3
Thrombocytopenia
3
childhood leukaemia
2
Case report
2
Castelman’s disease
2
Child
2
GATA2 Deficiency
2
Lymphedema
2
Myelodysplastic Syndrome
2
Paraneoplastic pemphigus
2
Primary Immunodeficiency Diseases
2
Therapy
2
acute lymphoblastic leukaemia
2
all-trans retinoic acid
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Erscheinungszeitraum
19
2020-
7
2010-2019
Erscheinungsjahr(e)
Von:
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Sprache
23
Englisch
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