Miller K - Search Results

1

Barton DE, Claustres M, Kozich V, Dequeker E, Fowler B, Hehir-Kwa JY, Miller K, Oosterwijk C, Peterlin B, van Ravenswaaij-Arts C, Zimmermann U, Zuffardi O, Hastings RJ. Barton DE, et al. Among authors: miller k. Eur J Hum Genet. 2016 Mar;24(3):330. doi: 10.1038/ejhg.2014.290. Epub 2015 Jan 14. Eur J Hum Genet. 2016. PMID: 25585701 Free PMC article. No abstract available.

2

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).

Claustres M, Kožich V, Dequeker E, Fowler B, Hehir-Kwa JY, Miller K, Oosterwijk C, Peterlin B, van Ravenswaaij-Arts C, Zimmermann U, Zuffardi O, Hastings RJ, Barton DE; European Society of Human Genetics. Claustres M, et al. Among authors: miller k. Eur J Hum Genet. 2014 Feb;22(2):160-70. doi: 10.1038/ejhg.2013.125. Epub 2013 Aug 14. Eur J Hum Genet. 2014. PMID: 23942201 Free PMC article.

3

The introduction of arrays in prenatal diagnosis: a special challenge.

Vetro A, Bouman K, Hastings R, McMullan DJ, Vermeesch JR, Miller K, Sikkema-Raddatz B, Ledbetter DH, Zuffardi O, van Ravenswaaij-Arts CM. Vetro A, et al. Among authors: miller k. Hum Mutat. 2012 Jun;33(6):923-9. doi: 10.1002/humu.22050. Epub 2012 Apr 16. Hum Mutat. 2012. PMID: 22508381

4

Prenatal diagnosis of an epignathus associated with a 49,XXXXY karyotype--a case report.

Staboulidou I, Miller K, Göhring G, Hillemanns P, Wüstemann M. Staboulidou I, et al. Among authors: miller k. Fetal Diagn Ther. 2008;24(3):313-7. doi: 10.1159/000160219. Epub 2008 Oct 3. Fetal Diagn Ther. 2008. PMID: 18832850

5

Comparison of Neurovascular Structures at Risk During Ankle Arthroscopy: A Cadaveric Study.

Sakkab R, Ivanova V, Jung M, Corley K, Kim JY, Sowda G, Miller K. Sakkab R, et al. Among authors: miller k. J Am Podiatr Med Assoc. 2024 Mar-Apr;114(2):21-220. doi: 10.7547/21-220. J Am Podiatr Med Assoc. 2024. PMID: 38758688

6

Long-term seizure diary tracking habits in clinical studies: Evidence from the Human Epilepsy Project.

Miller KR, Barnard S, Juarez-Colunga E, French JA, Pellinen J; Human Epilepsy Project Investigators. Miller KR, et al. Epilepsy Res. 2024 May 8;203:107379. doi: 10.1016/j.eplepsyres.2024.107379. Online ahead of print. Epilepsy Res. 2024. PMID: 38754255

7

Development and Delphi consensus validation of the Medication-Related Fall screening and scoring tool.

Saeed D, Carter G, Miller R, Darcy C, Miller K, Madden K, McKee H, Agnew J, Crawford P, Parsons C. Saeed D, et al. Among authors: miller k. Int J Clin Pharm. 2024 May 16. doi: 10.1007/s11096-024-01734-w. Online ahead of print. Int J Clin Pharm. 2024. PMID: 38753075

8

Development of second genetically distinct T-lymphoblastic leukemia in a pediatric patient.

Hultquist H, Rodriguez A, Ferreira JE, Placek A, Miller KP, Wood BL, Bhojwani D, Kapoor N, Raca G, Gaynon P, Kovach AE. Hultquist H, et al. Among authors: miller kp. Pediatr Blood Cancer. 2024 May 12:e31050. doi: 10.1002/pbc.31050. Online ahead of print. Pediatr Blood Cancer. 2024. PMID: 38736199 No abstract available.

9

A de novo germline RUNX1 variant preceding development of concurrent T-lymphoblastic leukemia and myelodysplastic syndrome.

Wang CP, Ferreira JE, Placek A, Aguayo-Hiraldo P, Raca G, Wood BL, Miller KP, Coates T, Freyer DR, Kovach AE. Wang CP, et al. Among authors: miller kp. Leuk Lymphoma. 2024 May 11:1-5. doi: 10.1080/10428194.2024.2347577. Online ahead of print. Leuk Lymphoma. 2024. PMID: 38733629

10

Distributed representations of prediction error signals across the cortical hierarchy are synergistic.

Gelens F, Äijälä J, Roberts L, Komatsu M, Uran C, Jensen MA, Miller KJ, Ince RAA, Garagnani M, Vinck M, Canales-Johnson A. Gelens F, et al. Among authors: miller kj. Nat Commun. 2024 May 10;15(1):3941. doi: 10.1038/s41467-024-48329-7. Nat Commun. 2024. PMID: 38729937 Free PMC article.

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