Publications by authors named "Roberto Lala"

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Intersexual Births: The Epistemology of Sex and Ethics of Sex Assignment.
Matteo Cresti, Elena Nave, Roberto Lala

J Bioeth Inq· December 2018

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Growth hormone-Insulin-like growth factor 1 axis hyperactivity on bone fibrous dysplasia in McCune-Albright Syndrome.
Daniele Tessaris, Alison M Boyce, Margaret Zacharin, Patrizia Matarazzo, Roberto Lala

Clin Endocrinol (Oxf)· July 2018

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Changing Pattern of Femoral Deformity During Growth in Polyostotic Fibrous Dysplasia of the Bone: An Analysis of 46 Cases.
Ernesto Ippolito, Matteo Benedetti Valentini, Roberto Lala, Fernando De Maio, Roberto Sorge

J Pediatr Orthop· April 2017

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Odontoiatric perspectives and osteonecrosis of the jaw as a possible adverse effect of bisphosphonates therapy in fibrous dysplasia and McCune-Albright syndrome.
Daniele Tessaris, Patrizia Matarazzo, Roberto Lala, Patrizia Defabianis

J Pediatr Endocrinol Metab· March 2016

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Improved sperm count and motility in young men surgically treated for cryptorchidism in the first year of life.
Francesca Feyles, Valentina Peiretti, Alessandro Mussa, Marco Manenti, Ferdinando Canavese, Roberto Lala

Eur J Pediatr Surg· October 2014

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Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism.
Patrizia Matarazzo, Gerdi Tuli, Ludovica Fiore, Alessandro Mussa, Francesca Feyles, Roberto Lala

J Pediatr Endocrinol Metab· January 2014

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20 novel point mutations and one large deletion in EXT1 and EXT2 genes: report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.
Michele Ciavarella, Michelina Coco, Filomena Baorda, Pietro Stanziale, Massimiliano Chetta, Roberto Lala

Gene· February 2013

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Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome.
Daniele Tessaris, Patrizia Matarazzo, Alessandro Mussa, Gerdi Tuli, Francesca Verna, Roberto Lala

Endocr J· July 2012

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Surgical enucleation of testicular leydigioma in a young child: case report and literature review.
Riccardo Guanà, Alessandro Mussa, Roberto Lala, Daniele Tessaris, Patrizia Maiullari Erasmo Tessiatore

J Pediatr Endocrinol Metab· January 2012

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Continuous subcutaneous hydrocortisone infusion (CSHI) in a young adolescent with congenital adrenal hyperplasia (CAH).
Gerdi Tuli, Ivana Rabbone, Silvia Einaudi, Valeria di Gianni, Daniele Tessaris, Roberto Lala

J Pediatr Endocrinol Metab· October 2011

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Cushing syndrome due to ectopic adrenocorticotropic hormone secretion in a 3-year-old child.
Patrizia Matarazzo, Gerdi Tuli, Daniele Tessaris, Francesca Verna, Ivana Rabbone, Roberto Lala

J Pediatr Endocrinol Metab· July 2011

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HDR syndrome: a novel "de novo" mutation in GATA3 gene.
Silvio Ferraris, Angelo Giovanni Del Monaco, Emanuela Garelli, Adriana Carando, Barbara De Vito, Roberto Lala

Am J Med Genet A· February 2009

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Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study.
Francesco Porta, Marco Spada, Roberto Lala, Alessandro Mussa

Ultrasound Med Biol· July 2008

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Multiple bone fractures in an 8-year-old child with cow's milk allergy and inappropriate calcium supplementation.
Giovanna Monti, Valentina Libanore, Letizia Marinaro, Roberto Lala, Roberto Miniero

Ann Nutr Metab· October 2007

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Persistent hyperestrogenism after precocious puberty in young females with McCune-Albright syndrome.
Roberto Lala, Maria Andreo, Angela Pucci, Patrizia Matarazzo

Pediatr Endocrinol Rev· August 2007

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Image diagnosis in McCune-Albright syndrome.
Claudio Defilippi, Domenico Chiappetta, Daniela Marzari, Alessandro Mussa, Roberto Lala

J Pediatr Endocrinol Metab· May 2006

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Laparoscopic management of ovarian cysts in peripheral precocious puberty of McCune-Albright syndrome.
Roberto Gesmundo, Riccardo Guanà, Laura Valfrè, Luisa De Sanctis, Patrizia Matarazzo, Roberto Lala

J Pediatr Endocrinol Metab· May 2006

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Genetics of McCune-Albright syndrome.
Luisa de Sanctis, Lisa Delmastro, Maria Chiara Russo, Patrizia Matarazzo, Roberto Lala

J Pediatr Endocrinol Metab· May 2006

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Bisphosphonate treatment of bone fibrous dysplasia in McCune-Albright syndrome.
Roberto Lala, Patrizia Matarazzo, Maria Andreo, Daniela Marzari, Jaele Bellone

J Pediatr Endocrinol Metab· May 2006

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McCune-Albright syndrome: persistence of autonomous ovarian hyperfunction during adolescence and early adult age.
Patrizia Matarazzo, Roberto Lala, Maria Andreo, Silvia Einaudi, Franco Altare

J Pediatr Endocrinol Metab· May 2006

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Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males.
Malgorzata Wasniewska, Filippo De Luca, Silvano Bertelloni, Patrizia Matarazzo, Giovanna Weber, Roberto Lala

J Pediatr· November 2004

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Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs.
Marco Di Stefano, Patrizia Chiabotto, Cristiana Roggia, Franco Garofalo, Roberto Lala

J Bone Miner Metab· July 2004

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Homeobox HOXA10 gene analysis in cryptorchidism.
Veronica Bertini, Silvano Bertelloni, Angelo Valetto, Roberto Lala, Carlo Foresta

J Pediatr Endocrinol Metab· January 2004

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Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
Luisa De Sanctis, Damiano Romagnolo, Martina Olivero, Fabio Buzi, Mohamad Maghnie, Roberto Lala

Pediatr Res· May 2003

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Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society.
Ernesto Ippolito, Edward W Bray, Alessandro Corsi, Fernando De Maio, Ulrich G Exner, Roberto Lala

J Pediatr Orthop B· May 2003

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