Publications by authors named "Marco Spinelli"

14Publications

Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia.

Acta Paediatr 2020 Oct 6. Epub 2020 Oct 6.

Department of Pediatric Onco-Hematology, San Gerardo Hospital, Fondazione MBBM, Università degli Studi di Milano-Bicocca, Monza, Italy.

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http://dx.doi.org/10.1111/apa.15593DOI Listing
October 2020

Female Genital Hair-Thread Tourniquet Syndrome: A Case Report and Literature Systematic Review.

J Pediatr Adolesc Gynecol 2020 Jul 18. Epub 2020 Jul 18.

Department of Gynecology, ASST Monza, San Gerardo University Hospital, Monza, Italy.

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http://dx.doi.org/10.1016/j.jpag.2020.07.007DOI Listing
July 2020

Corrigendum: A Narrative Approach to Describe QoL in Children With Chronic ITP.

Front Pediatr 2019;7:344. Epub 2019 Aug 26.

Foundation MBBM at San Gerardo Hospital, Pediatric Clinic University Milano-Bicocca, Monza, Italy.

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http://dx.doi.org/10.3389/fped.2019.00344DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718125PMC
August 2019

Lentiviral gene therapy corrects platelet phenotype and function in patients with Wiskott-Aldrich syndrome.

J Allergy Clin Immunol 2019 09 27;144(3):825-838. Epub 2019 Mar 27.

San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Division of Regenerative Medicine, Stem Cells and Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy; Milan Unit, Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2019.03.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721834PMC
September 2019

A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency.

Pediatr Allergy Immunol 2018 11 28;29(7):776-781. Epub 2018 Sep 28.

Department of Pathology, Institute for Molecular Medicine A. Nocivelli, Laboratory of Genetic Disorders of Childhood, University of Brescia, Brescia, Italy.

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http://doi.wiley.com/10.1111/pai.12968
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http://dx.doi.org/10.1111/pai.12968DOI Listing
November 2018

Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome.

Am J Med Genet A 2017 Feb 21;173(2):546-549. Epub 2016 Nov 21.

Clinical Genetic Pediatric Unit, Pediatric Department of MBBM Foundation, S. Gerardo Hospital, Monza, Italy.

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http://dx.doi.org/10.1002/ajmg.a.38057DOI Listing
February 2017

From Adjustment to Thriving: Exploring Well-Being in Young Adult Survivors of Childhood Cancer and Their Siblings.

J Adolesc Young Adult Oncol 2016 12 13;5(4):330-336. Epub 2016 Jun 13.

3 Pediatric Clinic, MBBM Foundation, Maria Letizia Verga Center , Monza, Italy .

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http://dx.doi.org/10.1089/jayao.2016.0005DOI Listing
December 2016

Thrombocytopenia and Cornelia de Lange syndrome: Still an enigma?

Am J Med Genet A 2016 Jan 5;170A(1):130-4. Epub 2015 Oct 5.

Department of Pediatrics, Monza Brianza per il Bambino e la sua Mamma (MBBM) Foundation, San Gerardo Hospital, Milano Bicocca University, Monza, Italy.

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http://dx.doi.org/10.1002/ajmg.a.37390DOI Listing
January 2016

Practices of pediatric oncology and hematology providers regarding fertility issues: a European survey.

Pediatr Blood Cancer 2014 Nov 25;61(11):2054-8. Epub 2014 Jul 25.

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

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http://dx.doi.org/10.1002/pbc.25163DOI Listing
November 2014