Intellectual and Developmental Disabilities: Denmark, Normalization, and De-Institutionalization

par Merrick, Joav, Uldall, Peter, Volther, Jakob
Publié 2014

A recurrent de novo CUX2 missense variant associated with intellectual disability, seizures, and autism spectrum disorder

par Barington, Maria, Risom, Lotte, Ek, Jakob, Uldall, Peter, Ostergaard, Elsebet
Publié dans Eur J Hum Genet (2018)

Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk

par Streja, Elani, Wu, Chunsen, Uldall, Peter, Grove, Jakob, Arah, Onyebuchi, Olsen, Jørn
Publié 2013

Parental infertility and cerebral palsy in children

par Zhu, Jin Liang, Hvidtjørn, Dorte, Basso, Olga, Obel, Carsten, Thorsen, Poul, Uldall, Peter, Olsen, Jørn
Publié 2010

Risk of Cerebral Palsy and Childhood Epilepsy Related to Infections before or during Pregnancy

par Wu, Chun S., Pedersen, Lars H., Miller, Jessica E., Sun, Yuelian, Streja, Elani, Uldall, Peter, Olsen, Jørn
Publié 2013

Disproportionate Fetal Growth and the Risk for Congenital Cerebral Palsy in Singleton Births

par Streja, Elani, Miller, Jessica E., Wu, Chunsen, Bech, Bodil H., Pedersen, Lars Henning, Schendel, Diana E., Uldall, Peter, Olsen, Jørn
Publié dans PLoS One (2015)

Phenotypic similarities and differences in patients with a p.Met112Ile mutation in SOX10

par Pingault, Veronique, Pierre-Louis, Laurence, Chaoui, Asma, Verloes, Alain, Sarrazin, Elisabeth, Brandberg, Goran, Bondurand, Nadege, Uldall, Peter, Manouvrier-Hanu, Sylvie
Publié dans Am J Med Genet A (2014)

Maternal thyroid disorder in pregnancy and risk of cerebral palsy in the child: a population-based cohort study

par Petersen, Tanja Gram, Andersen, Anne-Marie Nybo, Uldall, Peter, Paneth, Nigel, Feldt-Rasmussen, Ulla, Tollånes, Mette Christophersen, Strandberg-Larsen, Katrine
Publié dans BMC Pediatr (2018)

Parental socioeconomic status and risk of cerebral palsy in the child: evidence from two Nordic population-based cohorts

par Forthun, Ingeborg, Strandberg-Larsen, Katrine, Wilcox, Allen J, Moster, Dag, Petersen, Tanja Gram, Vik, Torstein, Lie, Rolv Terje, Uldall, Peter, Tollånes, Mette Christophersen
Publié dans Int J Epidemiol (2018)

Previous glucocorticoid treatment in childhood and adolescence is associated with long-term differences in subcortical grey matter volume and microstructure

par Holm, Sara Krøis, Madsen, Kathrine Skak, Vestergaard, Martin, Born, Alfred Peter, Paulson, Olaf B., Siebner, Hartwig Roman, Uldall, Peter, Baaré, William F.C.
Publié dans Neuroimage Clin (2019)

Ambient Exposure to Agricultural Pesticides during Pregnancy and Risk of Cerebral Palsy: A Population-Based Study in California

par Liew, Zeyan, von Ehrenstein, Ondine S., Ling, Chenxiao, Yuan, Yuying, Meng, Qi, Cui, Xin, Park, Andrew S., Uldall, Peter, Olsen, Jørn, Cockburn, Myles, Ritz, Beate
Publié dans Toxics (2020)

Maternal Infections during Pregnancy and Cerebral Palsy: A Population-based Cohort Study

par Miller, Jessica E., Pedersen, Lars Henning, Streja, Elani, Bech, Bodil H., Yeargin-Allsopp, Marshalyn, Van Naarden Braun, Kim, Schendel, Diana E., Christensen, Deborah, Uldall, Peter, Olsen, Jørn
Publié dans Paediatr Perinat Epidemiol (2013)

European study of frequency of participation of adolescents with and without cerebral palsy

par Michelsen, Susan I., Flachs, Esben M., Damsgaard, Mogens T., Parkes, Jacqueline, Parkinson, Kathryn, Rapp, Marion, Arnaud, Catherine, Nystrand, Malin, Colver, Allan, Fauconnier, Jerome, Dickinson, Heather O., Marcelli, Marco, Uldall, Peter
Publié 2014

Congenital cerebral palsy and prenatal exposure to self-reported maternal infections, fever, or smoking

par Streja, Elani, Miller, Jessica E., Bech, Bodil H., Greene, Naomi, Pedersen, Lars Henning, Yeargin-Allsopp, Marshalyn, Van Naarden Braun, Kim, Schendel, Diana E., Christensen, Deborah, Uldall, Peter, Olsen, Jørn
Publié dans Am J Obstet Gynecol (2013)

Use of paracetamol, ibuprofen or aspirin in pregnancy and risk of cerebral palsy in the child

par Petersen, Tanja Gram, Liew, Zeyan, Andersen, Anne-Marie Nybo, Andersen, Guro L, Andersen, Per Kragh, Martinussen, Torben, Olsen, Jørn, Rebordosa, Cristina, Tollånes, Mette Christophersen, Uldall, Peter, Wilcox, Allen J, Strandberg-Larsen, Katrine
Publié dans Int J Epidemiol (2018)

Electromagnetic source imaging in presurgical workup of patients with epilepsy: A prospective study

par Duez, Lene, Tankisi, Hatice, Hansen, Peter Orm, Sidenius, Per, Sabers, Anne, Pinborg, Lars H., Fabricius, Martin, Rásonyi, György, Rubboli, Guido, Pedersen, Birthe, Leffers, Anne-Mette, Uldall, Peter, Jespersen, Bo, Brennum, Jannick, Henriksen, Otto Mølby, Fuglsang-Frederiksen, Anders, Beniczky, Sándor
Publié dans Neurology (2019)

Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

par Møller, Rikke S., Larsen, Line H.G., Johannesen, Katrine M., Talvik, Inga, Talvik, Tiina, Vaher, Ulvi, Miranda, Maria J., Farooq, Muhammad, Nielsen, Jens E.K., Svendsen, Lene Lavard, Kjelgaard, Ditte B., Linnet, Karen M., Hao, Qin, Uldall, Peter, Frangu, Mimoza, Tommerup, Niels, Baig, Shahid M., Abdullah, Uzma, Born, Alfred P., Gellert, Pia, Nikanorova, Marina, Olofsson, Kern, Jepsen, Birgit, Marjanovic, Dragan, Al-Zehhawi, Lana I.K., Peñalva, Sofia J., Krag-Olsen, Bente, Brusgaard, Klaus, Hjalgrim, Helle, Rubboli, Guido, Pal, Deb K., Dahl, Hans A.
Publié dans Mol Syndromol (2016)

Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

par Neilson, Derek E., Adams, Mark D., Orr, Caitlin M.D., Schelling, Deborah K., Eiben, Robert M., Kerr, Douglas S., Anderson, Jane, Bassuk, Alexander G., Bye, Ann M., Childs, Anne-Marie, Clarke, Antonia, Crow, Yanick J., Di Rocco, Maja, Dohna-Schwake, Christian, Dueckers, Gregor, Fasano, Alfonso E., Gika, Artemis D., Gionnis, Dimitris, Gorman, Mark P., Grattan-Smith, Padraic J., Hackenberg, Annette, Kuster, Alice, Lentschig, Markus G., Lopez-Laso, Eduardo, Marco, Elysa J., Mastroyianni, Sotiria, Perrier, Julie, Schmitt-Mechelke, Thomas, Servidei, Serenella, Skardoutsou, Angeliki, Uldall, Peter, van der Knaap, Marjo S., Goglin, Karrie C., Tefft, David L., Aubin, Cristin, de Jager, Philip, Hafler, David, Warman, Matthew L.
Publié 2009

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

par Viollet, Louis, Glusman, Gustavo, Murphy, Kelley J., Newcomb, Tara M., Reyna, Sandra P., Sweney, Matthew, Nelson, Benjamin, Andermann, Frederick, Andermann, Eva, Acsadi, Gyula, Barbano, Richard L., Brown, Candida, Brunkow, Mary E., Chugani, Harry T., Cheyette, Sarah R., Collins, Abigail, DeBrosse, Suzanne D., Galas, David, Friedman, Jennifer, Hood, Lee, Huff, Chad, Jorde, Lynn B., King, Mary D., LaSalle, Bernie, Leventer, Richard J., Lewelt, Aga J., Massart, Mylynda B., Mérida, Mario R., Ptáček, Louis J., Roach, Jared C., Rust, Robert S., Renault, Francis, Sanger, Terry D., Sotero de Menezes, Marcio A., Tennyson, Rachel, Uldall, Peter, Zhang, Yue, Zupanc, Mary, Xin, Winnie, Silver, Kenneth, Swoboda, Kathryn J.
Publié dans PLoS One (2015)

Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

par Viollet, Louis, Glusman, Gustavo, Murphy, Kelley J., Newcomb, Tara M., Reyna, Sandra P., Sweney, Matthew, Nelson, Benjamin, Andermann, Frederick, Andermann, Eva, Acsadi, Gyula, Barbano, Richard L., Brown, Candida, Brunkow, Mary E., Chugani, Harry T., Cheyette, Sarah R., Collins, Abigail, DeBrosse, Suzanne D., Galas, David, Friedman, Jennifer, Hood, Lee, Huff, Chad, Jorde, Lynn B., King, Mary D., LaSalle, Bernie, Leventer, Richard J., Lewelt, Aga J., Massart, Mylynda B., Mérida, Mario R., Ptáček, Louis J., Roach, Jared C., Rust, Robert S., Renault, Francis, Sanger, Terry D., Sotero de Menezes, Marcio A., Tennyson, Rachel, Uldall, Peter, Zhang, Yue, Zupanc, Mary, Xin, Winnie, Silver, Kenneth, Swoboda, Kathryn J.
Publié dans PLoS One (2015)