Haas-Givler B - Search Results

1

The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome.

Finucane BM, Konar D, Haas-Givler B, Kurtz MB, Scott CI Jr. Finucane BM, et al. Dev Med Child Neurol. 1994 Jan;36(1):78-83. doi: 10.1111/j.1469-8749.1994.tb11770.x. Dev Med Child Neurol. 1994. PMID: 8132119

2

Genetics, mental retardation, and the forging of new alliances.

Finucane B, Haas-Givler B, Simon EW. Finucane B, et al. Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):66-72. doi: 10.1002/ajmg.c.10021. Am J Med Genet C Semin Med Genet. 2003. PMID: 12561060 Review.

3

A longitudinal follow-up study of autistic symptoms in children and adults with duplications of 15q11-13.

Simon EW, Haas-Givler B, Finucane B. Simon EW, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):463-467. doi: 10.1002/ajmg.b.31000. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19548260

4

Knowledge and perceptions about fragile X syndrome: implications for diagnosis, intervention, and research.

Finucane B, Haas-Givler B, Simon EW. Finucane B, et al. Among authors: haas givler b. Intellect Dev Disabil. 2013 Aug;51(4):226-36. doi: 10.1352/1934-9556-51.4.226. Intellect Dev Disabil. 2013. PMID: 23909584

5

Soy-Based Infant Formula is Associated with an Increased Prevalence of Comorbidities in Fragile X Syndrome.

Westmark CJ, Kniss C, Sampene E, Wang A, Milunovich A, Elver K, Hessl D, Talboy A, Picker J, Haas-Givler B, Esler A, Gropman AL, Uy R, Erickson C, Velinov M, Tartaglia N, Berry-Kravis EM. Westmark CJ, et al. Among authors: haas givler b. Nutrients. 2020 Oct 14;12(10):3136. doi: 10.3390/nu12103136. Nutrients. 2020. PMID: 33066511 Free PMC article.

6

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.

Kaufmann WE, Kidd SA, Andrews HF, Budimirovic DB, Esler A, Haas-Givler B, Stackhouse T, Riley C, Peacock G, Sherman SL, Brown WT, Berry-Kravis E. Kaufmann WE, et al. Among authors: haas givler b. Pediatrics. 2017 Jun;139(Suppl 3):S194-S206. doi: 10.1542/peds.2016-1159F. Pediatrics. 2017. PMID: 28814540 Free PMC article.

7

Best Practices in Fragile X Syndrome Treatment Development.

Erickson CA, Kaufmann WE, Budimirovic DB, Lachiewicz A, Haas-Givler B, Miller RM, Weber JD, Abbeduto L, Hessl D, Hagerman RJ, Berry-Kravis E. Erickson CA, et al. Among authors: haas givler b. Brain Sci. 2018 Dec 15;8(12):224. doi: 10.3390/brainsci8120224. Brain Sci. 2018. PMID: 30558274 Free PMC article.

8

Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort.

Berry-Kravis E, Filipink RA, Frye RE, Golla S, Morris SM, Andrews H, Choo TH, Kaufmann WE; FORWARD Consortium. Berry-Kravis E, et al. Front Pediatr. 2021 Dec 30;9:736255. doi: 10.3389/fped.2021.736255. eCollection 2021. Front Pediatr. 2021. PMID: 35036394 Free PMC article.

9

Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes.

Strauss KA, Carson VJ, Soltys K, Young ME, Bowser LE, Puffenberger EG, Brigatti KW, Williams KB, Robinson DL, Hendrickson C, Beiler K, Taylor CM, Haas-Givler B, Chopko S, Hailey J, Muelly ER, Shellmer DA, Radcliff Z, Rodrigues A, Loeven K, Heaps AD, Mazariegos GV, Morton DH. Strauss KA, et al. Among authors: haas givler b. Mol Genet Metab. 2020 Mar;129(3):193-206. doi: 10.1016/j.ymgme.2020.01.006. Epub 2020 Jan 16. Mol Genet Metab. 2020. PMID: 31980395 Free article.

10

APC7 mediates ubiquitin signaling in constitutive heterochromatin in the developing mammalian brain.

Ferguson CJ, Urso O, Bodrug T, Gassaway BM, Watson ER, Prabu JR, Lara-Gonzalez P, Martinez-Chacin RC, Wu DY, Brigatti KW, Puffenberger EG, Taylor CM, Haas-Givler B, Jinks RN, Strauss KA, Desai A, Gabel HW, Gygi SP, Schulman BA, Brown NG, Bonni A. Ferguson CJ, et al. Among authors: haas givler b. Mol Cell. 2022 Jan 6;82(1):90-105.e13. doi: 10.1016/j.molcel.2021.11.031. Epub 2021 Dec 22. Mol Cell. 2022. PMID: 34942119 Free PMC article.

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