Calvieri G - Search Results

1

Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis.

Alesi V, Dentici ML, Genovese S, Loddo S, Bellacchio E, Orlando V, Di Tommaso S, Catino G, Calacci C, Calvieri G, Pompili D, Ubertini G, Dallapiccola B, Capolino R, Novelli A. Alesi V, et al. Among authors: calvieri g. Int J Mol Sci. 2021 Jan 13;22(2):750. doi: 10.3390/ijms22020750. Int J Mol Sci. 2021. PMID: 33451138 Free PMC article.

2

A New Intronic Variant in ECEL1 in Two Patients with Distal Arthrogryposis Type 5D.

Alesi V, Sessini F, Genovese S, Calvieri G, Sallicandro E, Ciocca L, Mingoia M, Novelli A, Moi P. Alesi V, et al. Among authors: calvieri g. Int J Mol Sci. 2021 Feb 20;22(4):2106. doi: 10.3390/ijms22042106. Int J Mol Sci. 2021. PMID: 33672664 Free PMC article.

3

An additional patient with a homozygous mutation in DCPS contributes to the delination of Al-Raqad syndrome.

Alesi V, Capolino R, Genovesea S, Capriati T, Loddo S, Calvieri G, Calacci C, Diociaiuti A, Diamanti A, Novelli A, Dallapiccola B. Alesi V, et al. Among authors: calvieri g. Am J Med Genet A. 2018 Dec;176(12):2781-2786. doi: 10.1002/ajmg.a.40488. Epub 2018 Oct 5. Am J Med Genet A. 2018. PMID: 30289615 Review.

4

A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome.

Alesi V, Loddo S, Calì F, Orlando V, Genovese S, Ferretti D, Calacci C, Calvieri G, Falasca R, Ulgheri L, Drago F, Dallapiccola B, Baban A, Novelli A. Alesi V, et al. Among authors: calvieri g. Am J Med Genet A. 2019 Aug;179(8):1615-1621. doi: 10.1002/ajmg.a.61217. Epub 2019 May 30. Am J Med Genet A. 2019. PMID: 31145527 Review.

5

PPP1R21-related syndromic intellectual disability: Report of an adult patient and review.

Loddo S, Alesi V, Radio FC, Genovese S, Di Tommaso S, Calvieri G, Orlando V, Bertini E, Dentici ML, Novelli A, Dallapiccola B. Loddo S, et al. Among authors: calvieri g. Am J Med Genet A. 2020 Dec;182(12):3014-3022. doi: 10.1002/ajmg.a.61889. Epub 2020 Sep 27. Am J Med Genet A. 2020. PMID: 32985083 Review.

6

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.

Orlando V, Alesi V, Di Giacomo G, Canestrelli M, Calacci C, Nardone AM, Calvieri G, Liambo MT, Sallicandro E, Di Tommaso S, Di Gregorio MG, Corrado F, Barrano G, Niceta M, Dallapiccola B, Novelli A. Orlando V, et al. Among authors: calvieri g. Reprod Sci. 2021 Apr;28(4):1142-1149. doi: 10.1007/s43032-020-00419-9. Epub 2021 Jan 6. Reprod Sci. 2021. PMID: 33409881

7

Congenital heart defects in the recurrent 2q13 deletion syndrome.

Digilio MC, Dentici ML, Loddo S, Laino L, Calcagni G, Genovese S, Capolino R, Bottillo I, Calvieri G, Dallapiccola B, Marino B, Novelli A, Versacci P. Digilio MC, et al. Among authors: calvieri g. Eur J Med Genet. 2022 Jan;65(1):104381. doi: 10.1016/j.ejmg.2021.104381. Epub 2021 Nov 8. Eur J Med Genet. 2022. PMID: 34763108 Review.

8

Primary yolk sac tumor of the endometrium: a case report and review of the literature.

Rossi R, Stacchiotti D, Bernardini MG, Calvieri G, Lo Voi R. Rossi R, et al. Among authors: calvieri g. Am J Obstet Gynecol. 2011 Apr;204(4):e3-4. doi: 10.1016/j.ajog.2010.12.014. Epub 2011 Feb 23. Am J Obstet Gynecol. 2011. PMID: 21345404 Review.

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