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C Pignata

Showing results (51-60 of 76) with videos related to

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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 1, 1996
Severe, protracted intestinal cryptosporidiosis associated with interferon gamma deficiency: pediatric case reportM A Gomez Morales, C M Ausiello, A Guarino, et al.
European Journal of Neurology|February 23, 2008
Steroid-induced improvement of neurological signs in ataxia-telangiectasia patientsT Broccoletti, E Del Giudice, S Amorosi, et al.
Journal of Endocrinological Investigation|November 11, 2011
High intrafamilial variability in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: a case studyD Capalbo, A Fusco, G Aloj, et al.
Neuropediatrics|February 24, 2001
Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinaseE Del Giudice, L Gaetaniello, E Matrecano, et al.
American Journal of Medical Genetics. Part A|March 16, 2012
Noonan-like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestationsD Capalbo, D Melis, L De Martino, et al.
Clinical and Experimental Immunology|June 1, 1997
Combined immunodeficiency phenotype associated with inappropriate spontaneous and activation-induced apoptosisC Pignata, M Fiore, I Scotese, et al.
European Journal of Neurology|September 16, 2010
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasiaT Broccoletti, E Del Giudice, E Cirillo, et al.
Clinical Genetics|March 15, 2008
FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetusS Amorosi, M D'Armiento, G Calcagno, et al.
Clinical and Experimental Immunology|July 11, 2000
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in childrenC Pignata, M Alessio, U Ramenghi, et al.
Journal of Endocrinological Investigation|April 22, 2011
Molecular background and genotype-phenotype correlation in autoimmune-polyendocrinopathy-candidiasis-ectodermal-distrophy patients from Campania and in their relativesD Capalbo, C Mazza, R Giordano, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 1, 1996
Severe, protracted intestinal cryptosporidiosis associated with interferon gamma deficiency: pediatric case reportM A Gomez Morales, C M Ausiello, A Guarino, et al.
European Journal of Neurology|February 23, 2008
Steroid-induced improvement of neurological signs in ataxia-telangiectasia patientsT Broccoletti, E Del Giudice, S Amorosi, et al.
Journal of Endocrinological Investigation|November 11, 2011
High intrafamilial variability in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: a case studyD Capalbo, A Fusco, G Aloj, et al.
Neuropediatrics|February 24, 2001
Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinaseE Del Giudice, L Gaetaniello, E Matrecano, et al.
American Journal of Medical Genetics. Part A|March 16, 2012
Noonan-like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestationsD Capalbo, D Melis, L De Martino, et al.
Clinical and Experimental Immunology|June 1, 1997
Combined immunodeficiency phenotype associated with inappropriate spontaneous and activation-induced apoptosisC Pignata, M Fiore, I Scotese, et al.
European Journal of Neurology|September 16, 2010
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasiaT Broccoletti, E Del Giudice, E Cirillo, et al.
Clinical Genetics|March 15, 2008
FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetusS Amorosi, M D'Armiento, G Calcagno, et al.
Clinical and Experimental Immunology|July 11, 2000
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in childrenC Pignata, M Alessio, U Ramenghi, et al.
Journal of Endocrinological Investigation|April 22, 2011
Molecular background and genotype-phenotype correlation in autoimmune-polyendocrinopathy-candidiasis-ectodermal-distrophy patients from Campania and in their relativesD Capalbo, C Mazza, R Giordano, et al.
Pageof 8