Publications by authors named "Hamilton Cassinelli"

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Delayed diagnosis of X-linked hypophosphatemia in the absence of family history: a global unmet need.
Suma Uday, M Zulf Mughal, Hamilton Cassinelli, Pablo Florenzano, Erik A Imel

JBMR Plus· December 2025

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FSH and Sertoli Cell Biomarkers Accurately Distinguish Hypogonadotropic Hypogonadism From Self-limited Delayed Puberty.
Sebastián Castro, Lourdes Correa Brito, Patricia Bedecarrás, María Gabriela Ballerini, Gabriela Sansó, Hamilton Cassinelli

J Clin Endocrinol Metab· September 2025

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Guidelines for the prevention and treatment of glucocorticoid-induced osteoporosis in pediatrics.
Oscar Brunetto, Hamilton R Cassinelli, Graciela Espada, Gisela L Viterbo, Silvia M Meiorin

Arch Argent Pediatr· April 2024

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Serum Vitamin D Levels and Life-Threatening Respiratory Syncytial Virus Infection in Previously Healthy Infants.
F Martin Ferolla, E Walter Yfran, M Gabriela Ballerini, Ana Caratozzolo, Analía Toledano, Hamilton Cassinelli

J Infect Dis· September 2022

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[Rickets associated to the use of elemental formula: A case report].
Sebastián Castro, Carlos Velasco Suárez, Ana Vieites, Ignacio Bergadá, Hamilton Cassinelli

Arch Argent Pediatr· February 2021

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Burden of Disease in Patients With Tumor-Induced Osteomalacia.
Fernando Jerkovich, Selva Nuñez, Yamile Mocarbel, Analía Pignatta, Natalia Elías, Hamilton Cassinelli

JBMR Plus· February 2021

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[Osteoporosis-pseudoglioma Syndrome: a pediatric case of primary osteoporosis].
Débora Braslavsky, Paula Scaglia, Nora Sanguineti, Miriam Aza-Carmona, Julián Nevado Blanco, Hamilton Cassinelli

Arch Argent Pediatr· June 2020

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A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
Ana Claudia Keselman, Ayelen Martin, Paula Alejandra Scaglia, Nora María Sanguineti, Romina Armando, Hamilton Cassinelli

Eur J Endocrinol· November 2019

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Statement of Argentine pediatric endocrinologists on growth hormone interchangeability.
Guillermo Alonso, Viviana Balbi, Cristina Bazán de Casella, Alicia Belgorosky, Ignacio Bergadá, Hamilton Cassinelli

Arch Argent Pediatr· August 2019

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Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome.
Rathi Prasad, Irene Hadjidemetriou, Avinaash Maharaj, Eirini Meimaridou, Federica Buonocore, Hamilton Cassinelli

J Clin Invest· March 2017

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Global Consensus Recommendations on Prevention and Management of Nutritional Rickets.
Craig F Munns, Nick Shaw, Mairead Kiely, Bonny L Specker, Tom D Thacher, Hamilton Cassinelli

Horm Res Paediatr· November 2016

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Global Consensus Recommendations on Prevention and Management of Nutritional Rickets.
Craig F Munns, Nick Shaw, Mairead Kiely, Bonny L Specker, Tom D Thacher, Hamilton Cassinelli

J Clin Endocrinol Metab· February 2016

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Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis.
Abbhirami Rajagopal, Débora Braslavsky, James T Lu, Soledad Kleppe, Florencia Clément, Hamilton Cassinelli

J Clin Endocrinol Metab· November 2014

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Ocular manifestations of juvenile Paget disease.
Nathan M Kerr, Hamilton R Cassinelli, Linda A DiMeglio, Cristina Tau, Beyhan Tüysüz

Arch Ophthalmol· June 2010

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Establishment of testicular endocrine function impairment during childhood and puberty in boys with Klinefelter syndrome.
María Gabriela Bastida, Rodolfo A Rey, Ignacio Bergadá, Patricia Bedecarrás, Luz Andreone, Hamilton Cassinelli

Clin Endocrinol (Oxf)· December 2007

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Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.
Belinda Chong, Madhuri Hegde, Matthew Fawkner, Scott Simonet, Hamilton Cassinelli

J Bone Miner Res· December 2003

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