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Stefania Amorosi

Observed names: Amorosi, Stefania, S Amorosi, S. Amorosi
OpenAlex ID: A5081895506
FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetus
2008 · S Amorosi, M D’Armiento, et al. · Clinical Genetics · 64
Steroid‐induced improvement of neurological signs in ataxia‐telangiectasia patients
2008 · T. Broccoletti, E. Del Giudice, et al. · European Journal of Neurology · 62
In ataxia‐teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity
2009 · I. Russo, C. Cosentino, et al. · European Journal of Neurology · 52
FOXN1 mutation abrogates prenatal T-cell development in humans
2011 · I Vigliano, M Gorrese, et al. · Journal of Medical Genetics · 38
The Cellular Amount of the Common γ-Chain Influences Spontaneous or Induced Cell Proliferation
2009 · Stefania Amorosi, Ilaria Russo, et al. · The Journal of Immunology · 28
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Human ClinicalPhenotype Associated with FOXN1 Mutations
2009 · Claudio Pignata, Anna Fusco, et al. · Advances in experimental medicine and biology · 24
Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation
2010 · Stefania Amorosi, Ilaria Vigliano, et al. · Journal of the Neurological Sciences · 16
Functional Interaction of Common γ-Chain and Growth Hormone Receptor Signaling Apparatus
2006 · Marsilio Adriani, Corrado Garbi, et al. · The Journal of Immunology · 16
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Deficiency of FOXN1
2013 · Claudio Pignata, Anna Fusco, et al. · Oxford University Press eBooks
Novel Aspects in Immunodeficiencies
2009 · Amorosi, Stefania · Università degli Studi di Napoli Federico II
Shared Signaling Pathways Between Endocrine and Immune System Receptors: The Model of Gamma Chain
2008 · Claudio Pignata, Stefania Amorosi, et al. · Current Signal Transduction Therapy
F.69. A Novel Form of Hyper-IgM Syndrome
2008 · Teresa Broccoletti, Stefania Amorosi, et al. · Clinical Immunology
F.58. Î3-chain Provides a Spontaneous and GH-dependent Signal for Cell Cycle Progression Related to its Cellular Amount
2008 · Stefania Amorosi, Ilaria Russo, et al. · Clinical Immunology
I quattro paradossi delle nuove immunodeficienze congenite
2008 · Claudio Pignata, Stefania Amorosi, et al.
A novel form of hyper-IgM syndrome
2008 · Teresa Broccoletti, Stefania Amorosi, et al.
Analisi dell’ alterazione dei meccanismi di tolleranza periferica associata ad alta variabilità fenotipica.
2007 · I. Russo, Stefania Amorosi, et al.
Analisi della trasduzione del segnale via GHR in linee cellulari EBV di pazienti affetti da X-SCID e controlli.
2006 · Giuseppina Amodio, Stefania Amorosi, et al.
Works count: 17
Citation count: 300
H-index: 8
I10-index: 8
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