Works matching DE "CEREBRAL palsy genetics"

Results: 20

Cerebral Palsy and Polymorphism of the Chemokine CCL18 in Very Preterm Children.

Published in:

Neonatology (16617800), 2015, v. 108, n. 2, p. 124, doi. 10.1159/000430765

By:

Kallankari, Hanna;
Huusko, Johanna M.;
Kaukola, Tuula;
Ojaniemi, Marja;
Mahlman, Mari;
Marttila, Riitta;
Kingsmore, Stephen F.;
Haataja, Leena;
Lavoie, Pascal M.;
Synnes, anne;
Hallman, Mikko

Publication type:

Article

Genes determining the severity of cerebral palsy: the role of single nucleotide polymorphisms on the amount and structure of apolipoprotein E.

Published in:

Acta Paediatrica, 2015, v. 104, n. 7, p. 701, doi. 10.1111/apa.12983

By:

Lien, Espen;
Andersen, Guro;
Bao, Yongde;
Gordish‐Dressman, Heather;
Skranes, Jon S.;
Blackman, James A.;
Vik, Torstein

Publication type:

Article

Bone mineral density and insulin-like growth factor-1 in children with spastic cerebral palsy.

Published in:

Child's Nervous System, 2017, v. 33, n. 4, p. 625, doi. 10.1007/s00381-017-3346-9

By:

Nazif, H;
Shatla, R;
Elsayed, R;
Tawfik, E;
Osman, N;
Korra, S;
Ibrahim, A

Publication type:

Article

Research round-up.

Published in:: Learning Disability Practice, 2014, v. 17, n. 7, p. 19
Publication type:: Article

Association of COL4A1 gene polymorphisms with cerebral palsy in a Chinese Han population.

Published in:

Clinical Genetics, 2016, v. 90, n. 2, p. 149, doi. 10.1111/cge.12723

By:

Bi, D.;
Wang, H.;
Shang, Q.;
Xu, Y.;
Wang, F.;
Chen, M.;
Ma, C.;
Sun, Y.;
Zhao, X.;
Gao, C.;
Wang, L.;
Zhu, C.;
Xing, Q.

Publication type:

Article

About 14% of cerebral palsy cases may be tied to brain wiring genes.

Published in:

Neonatology Today, 2020, v. 15, n. 10, p. 86

By:

Goldstein, Mitchell

Publication type:

Article

Clinical digest. Familial risk of cerebral palsy confirmed but absolute risk is reassuringly low.

Published in:: Nursing Standard, 2014, v. 28, n. 49, p. 17, doi. 10.7748/ns.28.49.17.s24
Publication type:: Article

The genomic basis of cerebral palsy: a HuGE systematic literature review.

Published in:

Human Genetics, 2009, v. 126, n. 1, p. 149, doi. 10.1007/s00439-009-0638-5

By:

O'Callaghan, M. E.;
MacLennan, A. H.;
Haan, E. A.;
Dekker, G.

Publication type:

Article

Çocuklukta Engelliliğin En Sık Sebebi Nedir? Serebral Palsi Spektrumuna Nadir Hastalıklar Açısından Bakış.

Published in:

Medical Bulletin of Haseki / Haseki Tip Bulteni, 2020, v. 58, n. 4, p. 351, doi. 10.4274/haseki.galenos.2020.5984

By:

Akçakaya, Nihan Hande

Publication type:

Article

Genetic testing and the future of cerebral palsy malpractice cases: Would genetic testing have prevented this lawsuit?

Published in:

OBG Management, 2021, v. 33, n. 5, p. 37, doi. 10.12788/obgm.0091

By:

Sanfilippo, Joseph S.;
Smith, Steven R.

Publication type:

Article

Comparison of Digito-Palmar Dermatoglyphic Traits in Children with Cerebral Palsy and Their Close Family Members.

Published in:

Collegium Antropologicum, 2009, v. 33, n. 3, p. 925

By:

Polovina-Prološić, Tajana;
Miličić, Jasna;
Cvjetičanin, Miljenko;
Polovina, Andrea;
Polovina, Svetislav

Publication type:

Article

Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-Analysis.

Published in:

JAMA Pediatrics, 2025, v. 179, n. 2, p. 137, doi. 10.1001/jamapediatrics.2024.5059

By:

Lewis, Sara A.;
Chopra, Maya;
Cohen, Julie S.;
Bain, Jennifer M.;
Aravamuthan, Bhooma;
Carmel, Jason B.;
Fahey, Michael C.;
Segel, Reeval;
Wintle, Richard F.;
Zech, Michael;
May, Halie;
Haque, Nahla;
Fehlings, Darcy;
Srivastava, Siddharth;
Kruer, Michael C.

Publication type:

Article

Implications of Genetic Variants in Cerebral Palsy.

Published in:

2023

By:

Zhang, Ting;
Li, Tingsong

Publication type:

Letter

Whole-genome scale identification of methylation markers specific for cerebral palsy in monozygotic discordant twins.

Published in:

Molecular Medicine Reports, 2017, v. 16, n. 6, p. 9423, doi. 10.3892/mmr.2017.7800

By:

ZHE JIAO;
ZHIMEI JIANG;
JINGTAO WANG;
HUI XU;
QIANG ZHANG;
SHUANG LIU;
NING DU;
YUANYUAN ZHANG;
HONGBIN QIU

Publication type:

Article

Estimated Frequency of Genetic and Nongenetic Causes of Congenital Idiopathic Cerebral Palsy in West Sweden.

Published in:

Annals of Human Genetics, 2004, v. 68, n. 5, p. 515, doi. 10.1046/j.1529-8817.2004.00105.x

By:

Costeff, H.

Publication type:

Article

Research round-up.

Published in:: Learning Disability Practice, 2016, v. 19, n. 3, p. 15
Publication type:: Article

Mimickers of hypoxic-ischaemic brain injury in term neonates: What the radiologist should know.

Published in:

South African Journal of Radiology, 2024, v. 28, n. 1, p. 1, doi. 10.4102/sajr.v28i1.2810

By:

Misser, Shalendra K.;
Archary, Moherndran

Publication type:

Article

COL4A1 mutation in an Indian child presenting as 'Cerebral Palsy' mimic.

Published in:

Indian Journal of Radiology & Imaging, 2020, v. 30, n. 4, p. 500, doi. 10.4103/ijri.IJRI_274_20

By:

Shah, Siddharth;
Patel, Drushi

Publication type:

Article

A Tale of Two Boys: Case Report on Non-Consanguineous Siblings with Cerebral Palsy.

Published in:

Medicine & Health (Universiti Kebangsaan Malaysia), 2014, v. 9, n. 1, p. 74

By:

M., LEELAVATHI;
S., AHMAD;
J. L., LIM

Publication type:

Article

A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency.

Published in:

BMC Medical Genetics, 2014, v. 15, n. 1, p. 69, doi. 10.1186/s12881-014-0133-2

By:

Jameel, Muhammad;
Klar, Joakim;
Tariq, Muhammad;
Moawia, Abubakar;
Malik, Naveed Altaf;
Waseem, Syeda Seema;
Abdullah, Uzma;
Khan, Tahir Naeem;
Raininko, Raili;
Baig, Shahid Mahmood;
Dahl, Niklas

Publication type:

Article