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Items: 1 to 20 of 23

1.
Survival of neonates, infants, and children with birth defects: a population-based study in Texas, 1999–2018
Renata H. Benjamin, Joanne M. Nguyen, Mark A. Canfield, Charles J. Shumate, A.J. Agopian
Lancet Reg Health Am. 2023 Nov; 27: 100617. Published online 2023 Oct 18. doi: 10.1016/j.lana.2023.100617
PMCID:
PMC10589744
AbstractArticlePDF–1.3M
2.
Identifying environmental risk factors and gene-environment interactions in holoprosencephaly
Yonit A. Addissie, Angela Troia, Zoe C. Wong, Joshua L. Everson, Beth A. Kozel, Maximilian Muenke, Robert J. Lipinski, Kristen M.C. Malecki, Paul Kruszka
Birth Defects Res. Author manuscript; available in PMC 2022 Jul 17.
Published in final edited form as: Birth Defects Res. 2021 Jan 1; 113(1): 63–76. Published online 2020 Oct 28. doi: 10.1002/bdr2.1834
PMCID:
PMC9288838
AbstractArticlePDF–127K
3.
Concepts in Multifactorial Etiology of Developmental Disorders: Gene-Gene and Gene-Environment Interactions in Holoprosencephaly
Hsiao-Fan Lo, Mingi Hong, Robert S. Krauss
Front Cell Dev Biol. 2021; 9: 795194. Published online 2021 Dec 22. doi: 10.3389/fcell.2021.795194
PMCID:
PMC8727999
AbstractArticlePDF–1.1M
4.
Septopreoptic Holoprosencephaly: A Mild Subtype Associated with Midline Craniofacial Anomalies
J.S. Hahn, P.D. Barnes, N.J. Clegg, E.E. Stashinko
AJNR Am J Neuroradiol. 2010 Oct; 31(9): 1596–1601. doi: 10.3174/ajnr.A2123
PMCID:
PMC7965016
AbstractArticlePDF–1.0M
5.
Cohesin complex-associated holoprosencephaly
Paul Kruszka, Seth I Berger, Valentina Casa, Mike R Dekker, Jenna Gaesser, Karin Weiss, Ariel F Martinez, David R Murdock, Raymond J Louie, Eloise J Prijoles, Angie W Lichty, Oebele F Brouwer, Evelien Zonneveld-Huijssoon, Mark J Stephan, Jacob Hogue, Ping Hu, Momoko Tanima-Nagai, Joshua L Everson, Chitra Prasad, Anna Cereda, Maria Iascone, Allison Schreiber, Vickie Zurcher, Nicole Corsten-Janssen, Luis Escobar, Nancy J Clegg, Mauricio R Delgado, Omkar Hajirnis, Meena Balasubramanian, Hülya Kayserili, Matthew Deardorff, Raymond A Poot, Kerstin S Wendt, Robert J Lipinski, Maximilian Muenke
Brain. 2019 Sep; 142(9): 2631–2643. Published online 2019 Jul 23. doi: 10.1093/brain/awz210
PMCID:
PMC7245359
AbstractArticlePDF–714K
6.
Interventions to improve team effectiveness within health care: a systematic review of the past decade
Martina Buljac-Samardzic, Kirti D. Doekhie, Jeroen D. H. van Wijngaarden
Hum Resour Health. 2020; 18: 2. Published online 2020 Jan 8. doi: 10.1186/s12960-019-0411-3
PMCID:
PMC6950792
AbstractArticlePDF–788K
7.
Intraparenchymal hemorrhage and cerebral venous thrombosis in an adult with congenital porencephalic cyst presenting for generalized tonic-clonic seizures
Georges El Hasbani, Alaa Balaghi, Richard Assaker, Alberto Rojas, Marcelo Troya, Ahmad Kofahi, Jean Pierre Assaker, Chadi Diab, Husayn Al Husayni
Radiol Case Rep. 2020 Jan; 15(1): 95–99. Published online 2019 Nov 12. doi: 10.1016/j.radcr.2019.10.028
PMCID:
PMC6854081
AbstractArticlePDF–1.0M
8.
Alobar holoprosencephaly and Trisomy 13 (Patau syndrome)
Andressa Dias Costa, Regina Schultz, Sérgio Rosemberg
Autops Case Rep. 2013 Apr-Jun; 3(2): 5–10. Published online 2013 Jun 30. doi: 10.4322/acr.2013.012
PMCID:
PMC6673682
AbstractArticlePDF–1.5M
9.
Holoprosencephaly with Clefts: Data of 85 Patients, Treatment and Outcome: Part 1: History, Subdivisions, and Data on 85 Holoprosencephalic Cleft Patients
Engela M. Honey, Kurt W. Bütow, Roger Arthur Zwahlen
Ann Maxillofac Surg. 2019 Jan-Jun; 9(1): 140–145. doi: 10.4103/ams.ams_50_19
PMCID:
PMC6585219
AbstractArticlePDF–1.5M
10.
Case report: a novel mutation in ZIC2 in an infant with microcephaly, holoprosencephaly, and arachnoid cyst
Jianjun Xiong, Bingwu Xiang, Xiang Chen, Tao Cai
Medicine (Baltimore) 2019 Mar; 98(10): e14780. Published online 2019 Mar 8. doi: 10.1097/MD.0000000000014780
PMCID:
PMC6417543
AbstractArticlePDF–452K
11.
Syndromes Associated with Holoprosencephaly
Paul Kruszka, Maximilian Muenke
Am J Med Genet C Semin Med Genet. Author manuscript; available in PMC 2019 Jun 1.
Published in final edited form as: Am J Med Genet C Semin Med Genet. 2018 Jun; 178(2): 229–237. Published online 2018 May 17. doi: 10.1002/ajmg.c.31620
PMCID:
PMC6125175
AbstractArticlePDF–251K
12.
Molecular Testing in Holoprosencephaly
Paul Kruszka, Ariel F. Martinez, Maximilian Muenke
Am J Med Genet C Semin Med Genet. Author manuscript; available in PMC 2019 Jun 1.
Published in final edited form as: Am J Med Genet C Semin Med Genet. 2018 Jun; 178(2): 187–193. Published online 2018 May 17. doi: 10.1002/ajmg.c.31617
PMCID:
PMC6125165
AbstractArticlePDF–329K
13.
Middle interhemispheric variant of holoprosencephaly: A rare midline malformation
P. Prathiba Rajalakshmi, Ankur Gadodia, P. Priyatharshini
J Pediatr Neurosci. 2015 Jul-Sep; 10(3): 244–246. doi: 10.4103/1817-1745.165678
PMCID:
PMC4611894
AbstractArticle
14.
Septo-optic dysplasia: Magnetic Resonance Imaging findings
Vinay K. Maurya, R. Ravikumar, M. Bhatia, Roma Rai
Med J Armed Forces India. 2015 Jul; 71(3): 287–289. Published online 2015 Jun 29. doi: 10.1016/j.mjafi.2015.04.013
PMCID:
PMC4534561
AbstractArticlePDF–637K
15.
Holoprosencephaly: signalling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans
Anna Petryk, Daniel Graf, Ralph Marcucio
Wiley Interdiscip Rev Dev Biol. Author manuscript; available in PMC 2016 Jan 1.
Published in final edited form as: Wiley Interdiscip Rev Dev Biol. 2015 Jan; 4(1): 17–32. Published online 2014 Oct 22. doi: 10.1002/wdev.161
PMCID:
PMC4268052
AbstractArticlePDF–1.6M
16.
Holoprosencephaly: recommendations for diagnosis and management
Emily F. Kauvar, Maximilian Muenke
Curr Opin Pediatr. Author manuscript; available in PMC 2014 Aug 13.
Published in final edited form as: Curr Opin Pediatr. 2010 Dec; 22(6): 687–695. doi: 10.1097/MOP.0b013e32833f56d5
PMCID:
PMC4131980
AbstractArticlePDF–1.9M
17.
Holoprosencephaly: A Guide to Diagnosis and Clinical Management
Manu S Raam, Benjamin D Solomon, Maximilian Muenke
Indian Pediatr. Author manuscript; available in PMC 2014 Aug 13.
Published in final edited form as: Indian Pediatr. 2011 Jun; 48(6): 457–466. doi: 10.1007/s13312-011-0078-x
PMCID:
PMC4131946
AbstractArticlePDF–285K
18.
Holoprosencephaly with Multiple Anomalies of the Craniofacial Bones-An Autopsy Report
E. Aruna, V. Kalyan Chakravarthy, D. Naveen Chandar Rao, D. Ranga Rao
J Clin Diagn Res. 2013 Aug; 7(8): 1722–1724. Published online 2013 Aug 1. doi: 10.7860/JCDR/2013/5734.3268
PMCID:
PMC3782948
AbstractArticlePDF–304K
19.
Hydranencephaly: A Rare Cause of an Enlarging Head Size in an Infant
Mohd Khalid, Saifullah Khalid, Samreen Zaheer, Navneet Redhu, Ekramullah
N Am J Med Sci. 2012 Oct; 4(10): 520–522. doi: 10.4103/1947-2714.102015
PMCID:
PMC3482792
ArticlePDF–490K
20.
Molecular Analysis of the Noggin (NOG) Gene in Holoprosencephaly Patients
Kshitij Srivastava, Ping Hu, Benjamin D. Solomon, Jeffrey E. Ming, Erich Roessler, Maximilian Muenke
Mol Genet Metab. Author manuscript; available in PMC 2013 Jun 1.
Published in final edited form as: Mol Genet Metab. 2012 Jun; 106(2): 241–243. Published online 2012 Mar 21. doi: 10.1016/j.ymgme.2012.03.008
PMCID:
PMC3356444
AbstractArticlePDF–38K

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