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Page 1
Global Consensus Recommendations on Prevention and Management of Nutritional Rickets.
Munns CF, Shaw N, Kiely M, Specker BL, Thacher TD, Ozono K, Michigami T, Tiosano D, Mughal MZ, Mäkitie O, Ramos-Abad L, Ward L, DiMeglio LA, Atapattu N, Cassinelli H, Braegger C, Pettifor JM, Seth A, Idris HW, Bhatia V, Fu J, Goldberg G, Sävendahl L, Khadgawat R, Pludowski P, Maddock J, Hyppönen E, Oduwole A, Frew E, Aguiar M, Tulchinsky T, Butler G, Högler W. Munns CF, et al. Among authors: cassinelli h. J Clin Endocrinol Metab. 2016 Feb;101(2):394-415. doi: 10.1210/jc.2015-2175. Epub 2016 Jan 8. J Clin Endocrinol Metab. 2016. PMID: 26745253 Free PMC article. Review.
Ocular manifestations of juvenile Paget disease.
Kerr NM, Cassinelli HR, DiMeglio LA, Tau C, Tüysüz B, Cundy T, Vincent AL. Kerr NM, et al. Arch Ophthalmol. 2010 Jun;128(6):698-703. doi: 10.1001/archophthalmol.2010.76. Arch Ophthalmol. 2010. PMID: 20547946
[Rickets associated to the use of elemental formula: A case report].
Castro S, Velasco Suárez C, Vieites A, Bergadá I, Cassinelli H. Castro S, et al. Among authors: cassinelli h. Arch Argent Pediatr. 2021 Feb;119(1):e49-e53. doi: 10.5546/aap.2021.e49. Arch Argent Pediatr. 2021. PMID: 33458991 Free article. Spanish.
[Osteoporosis-pseudoglioma Syndrome: a pediatric case of primary osteoporosis].
Braslavsky D, Scaglia P, Sanguineti N, Aza-Carmona M, Nevado Blanco J, Lapunzina Badia PD, Fernández MDC, Ruiz O, Carmona A, Szlago M, Arberas C, Cassinelli H, Heath K, Rey R, Bergadá I. Braslavsky D, et al. Among authors: cassinelli h. Arch Argent Pediatr. 2020 Jun;118(3):e300-e304. doi: 10.5546/aap.2020.e300. Arch Argent Pediatr. 2020. PMID: 32470270 Free article. Spanish.
Statement of Argentine pediatric endocrinologists on growth hormone interchangeability.
Alonso G, Balbi V, Bazán de Casella C, Belgorosky A, Bergadá I, Brunetto O, Cassinelli H, Ciaccio M, Keselman A, Miras MB, Morín A; Comité Nacional de Endocrinología Pediátrica. Alonso G, et al. Among authors: cassinelli h. Arch Argent Pediatr. 2019 Aug 1;117(4):212-215. doi: 10.5546/aap.2019.eng.213. Arch Argent Pediatr. 2019. PMID: 31339262 Free article. English, Spanish. No abstract available.
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency.
Keselman AC, Martin A, Scaglia PA, Sanguineti NM, Armando R, Gutiérrez M, Braslavsky D, Ballerini MG, Ropelato MG, Ramirez L, Landi E, Domené S, Castro JF, Cassinelli H, Casali B, Del Rey G, Barros ÁC, Nevado Blanco J, Domené H, Jasper H, Arberas C, Rey RA, Lapunzina-Badía P, Bergadá I, Pennisi PA. Keselman AC, et al. Among authors: cassinelli h. Eur J Endocrinol. 2019 Nov;181(5):K43-K53. doi: 10.1530/EJE-19-0563. Eur J Endocrinol. 2019. PMID: 31539878
Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis.
Rajagopal A, Braslavsky D, Lu JT, Kleppe S, Clément F, Cassinelli H, Liu DS, Liern JM, Vallejo G, Bergadá I, Gibbs RA, Campeau PM, Lee BH. Rajagopal A, et al. Among authors: cassinelli h. J Clin Endocrinol Metab. 2014 Nov;99(11):E2451-6. doi: 10.1210/jc.2014-1517. Epub 2014 Jul 22. J Clin Endocrinol Metab. 2014. PMID: 25050900 Free PMC article.
23 results