Kline AD - Search Results

1

Agreement between parent-proxy and child self-report in pediatric hypermobile Ehlers-Danlos syndrome.

Wang Y, Clemens JL, Muriello M, Mu W, Smith CH, Tran PT, Rowe PC, Francomano C, Kline AD, Bodurtha J. Wang Y, et al. Among authors: kline ad. J Child Health Care. 2022 Sep 21:13674935221110081. doi: 10.1177/13674935221110081. Online ahead of print. J Child Health Care. 2022. PMID: 36128922

2

Pain and sleep quality in children with non-vascular Ehlers-Danlos syndromes.

Muriello M, Clemens JL, Mu W, Tran PT, Rowe PC, Smith CH, Francomano C, Bodurtha J, Kline AD. Muriello M, et al. Among authors: kline ad. Am J Med Genet A. 2018 Sep;176(9):1858-1864. doi: 10.1002/ajmg.a.40371. Epub 2018 Sep 4. Am J Med Genet A. 2018. PMID: 30178919 Free PMC article.

3

Factors affecting quality of life in children and adolescents with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders.

Mu W, Muriello M, Clemens JL, Wang Y, Smith CH, Tran PT, Rowe PC, Francomano CA, Kline AD, Bodurtha J. Mu W, et al. Among authors: kline ad. Am J Med Genet A. 2019 Apr;179(4):561-569. doi: 10.1002/ajmg.a.61055. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703284 Free PMC article.

4

Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment.

Roshan Lal TR, Kliewer MA, Lopes T, Rebsamen SL, O'Connor J, Grados MA, Kimball A, Clemens J, Kline AD. Roshan Lal TR, et al. Among authors: kline ad. Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):190-7. doi: 10.1002/ajmg.c.31503. Epub 2016 May 10. Am J Med Genet C Semin Med Genet. 2016. PMID: 27164360 Free PMC article.

5

Further Characterization of SMC1A Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome.

Barañano KW, Kimball A, Fong SL, Egense AS, Hudon C, Kline AD. Barañano KW, et al. Among authors: kline ad. J Child Neurol. 2022 Apr;37(5):390-396. doi: 10.1177/08830738221081244. Epub 2022 Mar 3. J Child Neurol. 2022. PMID: 35238682

6

Neurobehavioral and developmental profiles: genotype-phenotype correlations in individuals with Cornelia de Lange syndrome.

Ng R, O'Connor J, Summa D, Kline AD. Ng R, et al. Among authors: kline ad. Orphanet J Rare Dis. 2024 Mar 10;19(1):111. doi: 10.1186/s13023-024-03104-1. Orphanet J Rare Dis. 2024. PMID: 38462617 Free PMC article.

7

Repetitive and Self-injurious Behaviors in Children with Cornelia de Lange Syndrome.

Srivastava S, Clark B, Landy-Schmitt C, Offermann EA, Kline AD, Wilkinson ST, Grados MA. Srivastava S, et al. Among authors: kline ad. J Autism Dev Disord. 2021 May;51(5):1748-1758. doi: 10.1007/s10803-020-04617-x. J Autism Dev Disord. 2021. PMID: 32809170

8

A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies.

Kline AD, Griffin CA, Haddadin MH, Chudoba I, Morsberger LA, Hawkins AL, Amato RS, Munshi G, Cohen MM. Kline AD, et al. Am J Med Genet A. 2004 Aug 30;129A(2):124-9. doi: 10.1002/ajmg.a.30130. Am J Med Genet A. 2004. PMID: 15316975

9

Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance.

Kline AD, Krantz ID, Sommer A, Kliewer M, Jackson LG, FitzPatrick DR, Levin AV, Selicorni A. Kline AD, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1287-96. doi: 10.1002/ajmg.a.31757. Am J Med Genet A. 2007. PMID: 17508425 Review.

10

Natural history of aging in Cornelia de Lange syndrome.

Kline AD, Grados M, Sponseller P, Levy HP, Blagowidow N, Schoedel C, Rampolla J, Clemens DK, Krantz I, Kimball A, Pichard C, Tuchman D. Kline AD, et al. Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):248-60. doi: 10.1002/ajmg.c.30137. Am J Med Genet C Semin Med Genet. 2007. PMID: 17640042 Free PMC article. Review.

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