Role of Rac and Cdc42 in lysophosphatidic acid-mediated cyclo-oxygenase-2 gene expression.

nork Hahn, Angelika, Barth, Holger, Kress, Michaela, Mertens, Peter R, Goppelt-Struebe, Margarete
Argitaratua 2002

A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

nork Bendahhou, Saïd, Cummins, Theodore R., Hahn, Angelika F., Langlois, Sylvie, Waxman, Stephen G., Ptácek, Louis J.
Argitaratua 2000

Novel NALCN variant: altered respiratory and circadian rhythm, anesthetic sensitivity

nork Lozic, Bernarda, Johansson, Stefan, Lovric Kojundzic, Sanja, Markic, Josko, Knappskog, Per Morten, Hahn, Angelika F., Boman, Helge
Argitaratua izan da Ann Clin Transl Neurol (2016)

Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

nork Valentino, Maria Lucia, Martí, Ramon, Tadesse, Saba, Lopez, Luis Carlos, Manes, Jose L., Lyzak, Judy, Hahn, Angelika, Carelli, Valerio, Hirano, Michio
Argitaratua 2007

Unusual Stüve-Wiedemann syndrome with complete maternal chromosome 5 isodisomy

nork Melone, Mariarosa A B, Pellegrino, Michael J, Nolano, Maria, Habecker, Beth A, Johansson, Stefan, Nathanson, Neil M, Knappskog, Per M, Hahn, Angelika F, Boman, Helge
Argitaratua izan da Ann Clin Transl Neurol (2014)

Inactivation of cardiotrophin-like cytokine, a second ligand for ciliary neurotrophic factor receptor, leads to cold-induced sweating syndrome in a patient

nork Rousseau, François, Gauchat, Jean-François, McLeod, James G., Chevalier, Sylvie, Guillet, Catherine, Guilhot, Florence, Cognet, Isabelle, Froger, Josy, Hahn, Angelika F., Knappskog, Per M., Gascan, Hugues, Boman, Helge
Argitaratua 2006

Episodic ataxia type 1: clinical characterization, quality of life and genotype–phenotype correlation

nork Graves, Tracey D., Cha, Yoon-Hee, Hahn, Angelika F., Barohn, Richard, Salajegheh, Mohammed K., Griggs, Robert C., Bundy, Brian N., Jen, Joanna C., Baloh, Robert W., Hanna, Michael G.
Argitaratua 2014

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

nork Tristani-Firouzi, Martin, Jensen, Judy L., Donaldson, Matthew R., Sansone, Valeria, Meola, Giovanni, Hahn, Angelika, Bendahhou, Said, Kwiecinski, Hubert, Fidzianska, Anna, Plaster, Nikki, Fu, Ying-Hui, Ptacek, Louis J., Tawil, Rabi
Argitaratua 2002

Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2

nork Fogel, Brent L., Cho, Ellen, Wahnich, Amanda, Gao, Fuying, Becherel, Olivier J., Wang, Xizhe, Fike, Francesca, Chen, Leslie, Criscuolo, Chiara, De Michele, Giuseppe, Filla, Alessandro, Collins, Abigail, Hahn, Angelika F., Gatti, Richard A., Konopka, Genevieve, Perlman, Susan, Lavin, Martin F., Geschwind, Daniel H., Coppola, Giovanni
Argitaratua 2014

Familial Cortical Myoclonus with a Mutation in NOL3

nork Russell, Jonathan F., Steckley, Jamie L., Coppola, Giovanni, Hahn, Angelika F.G., Howard, MacKenzie A., Kornberg, Zachary, Huang, Alden, Mirsattari, Seyed M., Merriman, Barry, Klein, Eric, Choi, Murim, Lee, Hsien-Yang, Kirk, Andrew, Nelson-Williams, Carol, Gibson, Gillian, Baraban, Scott C., Lifton, Richard P., Geschwind, Daniel H., Fu, Ying-Hui, Ptáček, Louis J.
Argitaratua 2012