Shur N - Search Results

1

Editorial: Medical genetics, expert medical testimony, and suspected child abuse cases: a call for evidence-based standards in clinic and the courtroom.

Shur N, Robin NH. Shur N, et al. Curr Opin Pediatr. 2021 Feb 1;33(1):1-2. doi: 10.1097/MOP.0000000000000987. Curr Opin Pediatr. 2021. PMID: 33337605 No abstract available.

2

A case of broken bones and systems: The threat of irresponsible testimony.

Shur N. Shur N. Am J Med Genet A. 2019 Mar;179(3):429-434. doi: 10.1002/ajmg.a.61043. Epub 2019 Jan 29. Am J Med Genet A. 2019. PMID: 30697977

3

Genetic consultations in cases of unexplained fractures and haemorrhage: an evidence-based approach.

Shur N, Summerlin ML, Robin NH, Moreno-Mendelson A, Shalaby-Rana E, Hinds T. Shur N, et al. Curr Opin Pediatr. 2021 Feb 1;33(1):3-18. doi: 10.1097/MOP.0000000000000986. Curr Opin Pediatr. 2021. PMID: 33337606 Review.

4

Invited commentary: His life was lost but his heart still beats: In honor of children harmed by child abuse.

Shur N, Hinds T, Shalaby-Rana E, Tinkle B, Frasier L, Bulas D, Summar M, Jackson A. Shur N, et al. Am J Med Genet A. 2019 Dec;179(12):2329-2332. doi: 10.1002/ajmg.a.61348. Epub 2019 Sep 29. Am J Med Genet A. 2019. PMID: 31565855 No abstract available.

5

Society for Pediatric Radiology (SPR) Child Abuse Committee response regarding Miller, Stolfi and Ayoub's flawed theories about child abuse and metabolic bone disease.

Brown SD, Moreno JA, Shur N, Servaes S. Brown SD, et al. Among authors: shur n. J Pediatr Endocrinol Metab. 2020 Apr 28;33(4):547-548. doi: 10.1515/jpem-2019-0544. J Pediatr Endocrinol Metab. 2020. PMID: 32084006 No abstract available.

6

Pediatric medical genetics house call: Telemedicine for the next generation of patients and providers.

Cohen AJ, Shur N, Starin D, MacLeod E, Roshan Lal T, Leon E, Regier DS. Cohen AJ, et al. Among authors: shur n. Am J Med Genet C Semin Med Genet. 2021 Mar;187(1):55-63. doi: 10.1002/ajmg.c.31882. Epub 2021 Jan 11. Am J Med Genet C Semin Med Genet. 2021. PMID: 33427371

7

Rapid deployment of a telemedicine care model for genetics and metabolism during COVID-19.

Shur N, Atabaki SM, Kisling MS, Tabarani A, Williams C, Fraser JL, S Regier D, Summar M; Rare Disease Institute. Shur N, et al. Am J Med Genet A. 2021 Jan;185(1):68-72. doi: 10.1002/ajmg.a.61911. Epub 2020 Oct 14. Am J Med Genet A. 2021. PMID: 33051968 Free PMC article.

8

Ehlers-Danlos syndrome: what the radiologist needs to know.

George MP, Shur NE, Peréz-Rosselló JM. George MP, et al. Pediatr Radiol. 2021 May;51(6):1023-1028. doi: 10.1007/s00247-020-04856-1. Epub 2021 May 17. Pediatr Radiol. 2021. PMID: 33999243 Review.

9

Genetic causes of fractures and subdural hematomas: fact versus fiction.

Shur NE, Summerlin ML, McIntosh BJ, Shalaby-Rana E, Hinds TS. Shur NE, et al. Pediatr Radiol. 2021 May;51(6):1029-1043. doi: 10.1007/s00247-020-04865-0. Epub 2021 May 17. Pediatr Radiol. 2021. PMID: 33999244 Review.

10

The past, present, and future of child growth monitoring: A review and primer for clinical genetics.

Shur N, Tigranyan A, Daymont C, Regier DS, Raturi S, Roshan Lal T, Cleary K, Summar M. Shur N, et al. Am J Med Genet A. 2023 Apr;191(4):948-961. doi: 10.1002/ajmg.a.63102. Epub 2023 Jan 28. Am J Med Genet A. 2023. PMID: 36708136 Review.

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