Showing 1 - 20 results of 59 for search 'T. Diociaiuti', query time: 0.05s
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Membranous aplasia cutis congenita in trisomy 18 by Francisco Cammarata-Scalisi, Andrea Diociaiuti, Blanca de Guerrero, Colin Eric Willoughby, Michele Callea
Published 2020-08-01
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PIK3CA-related overgrowth with an uncommon phenotype: case report by Roberta Rotunno, Andrea Diociaiuti, Elisa Pisaneschi, Claudia Carnevale, Marialisa Dentici, May El Hachem
Published 2022-05-01
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ITGB4-mutated Junctional Epidermolysis Bullosa without Pyloric Atresia Presenting with Severe Urinary Involvement and Late-onset Minimal Skin Fragility: Diagnostic and Therapeutic... by Girolamo Mattioli, Andrea Diociaiuti, Sabrina Rossi, Giovanna Zambruno, Marcello Carlucci, Elisa Pisaneschi, May El Hachem
Published 2022-05-01
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Correction to: Italian translation, cultural adaptation, and pilot testing of a questionnaire to assess family burden in inherited ichthyoses by May El Hachem, Damiano Abeni, Andrea Diociaiuti, Roberta Rotunno, Francesco Gesualdo, Giovanna Zambruno, Christine Bodemer
Published 2020-03-01
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Angioma serpiginosum: a case report and review of the literature by Andrea Diociaiuti, Mario Cutrone, Roberta Rotunno, Rita De Vito, Iria Neri, Elisa Pisaneschi, May El Hachem
Published 2019-04-01
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Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation by Andrea Diociaiuti, Roberta Caruso, Silvia Ricci, Rita De Vito, Luisa Strocchio, Daniele Castiglia, Giovanna Zambruno, May El Hachem
Published 2022-05-01
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Color Doppler Evaluation of Arterial Resistive Index in Infantile Hemangioma: A Useful Parameter to Monitor the Response to Oral Propranolol? by George Koshy Parapatt, Teresa Oranges, Guglielmo Paolantonio, Lucilla Ravà, Simona Giancristoforo, Andrea Diociaiuti, May El Hachem, Massimo Rollo
Published 2021-12-01
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Next Generation Sequencing Uncovers a Rare Case of X-linked Ichthyosis in an Adopted Girl Homozygous for a Novel Nonsense Mutation in the STS Gene by Andrea Diociaiuti, Adriano Angioni, Elisa Pisaneschi, Maria Margollicci, Renata Boldrini, Viola Alesi, Antonio Novelli, Giovanna Zambruno, May El Hachem
Published 2019-05-01
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Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review by Roberta Rotunno, Andrea Diociaiuti, Maria Lisa Dentici, Martina Rinelli, Michele Callea, Chiara Retrosi, Giovanna Zambruno, Emanuele Bellacchio, May El Hachem
Published 2021-05-01
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