Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice

Milka Pringsheim; Diana Mitter; Simone Schroeder; Rita Warthemann; Kim Pluemacher; Gerhard Kluger; Martina Baethmann; Thomas Bast; Sarah Braun; Hans-Martin Buettel; Elizabeth Conover; Carolina Courage; Alexandre N. Datta; Angelika Eger; Theresa A. Grebe; Annette Hasse-Wittmer; Marion Heruth; Karen Hoeft; Angela M. Kaindl; Stephanie Karch; Torsten Kautzky; Georg C. Korenke; Bernd Kruse; Richard E. Lutz; Heymut Omran; Steffi Patzer; Heike Philippi; Keri Ramsey; Tina Rating; Angelika Riess; Mareike Schimmel; Rachel Westman; Frank-Martin Zech; Birgit Zirn; Pauline A. Ulmke; Godwin Sokpor; Tran Tuoc; Andreas Leha; Martin Staudt; Knut Brockmann

doi:10.1002/acn3.735

Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice

Milka Pringsheim, Diana Mitter, Simone Schroeder, Rita Warthemann, Kim Pluemacher, Gerhard Kluger, Martina Baethmann, Thomas Bast, Sarah Braun, Hans-Martin Buettel, Elizabeth Conover, Carolina Courage, Alexandre N. Datta, Angelika Eger, Theresa A. Grebe, Annette Hasse-Wittmer, Marion Heruth, Karen Hoeft, Angela M. Kaindl, Stephanie KarchTorsten Kautzky, Georg C. Korenke, Bernd Kruse, Richard E. Lutz, Heymut Omran, Steffi Patzer, Heike Philippi, Keri Ramsey, Tina Rating, Angelika Riess, Mareike Schimmel, Rachel Westman, Frank-Martin Zech, Birgit Zirn, Pauline A. Ulmke, Godwin Sokpor, Tran Tuoc, Andreas Leha, Martin Staudt, Knut Brockmann

Tutkimustuotos: Artikkelijulkaisu › Artikkeli › Tieteellinen › vertaisarvioitu

Alkuperäiskieli	englanti
Lehti	Annals of Clinical and Translational Neurology
Vuosikerta	6
Numero	4
Sivut	655-668
Sivumäärä	14
ISSN	2328-9503
DOI - pysyväislinkit	https://doi.org/10.1002/acn3.735
Tila	Julkaistu - huhtik. 2019
OKM-julkaisutyyppi	A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu

Tieteenalat

3112 Neurotieteet
3124 Neurologia ja psykiatria

Pääsy asiakirjaan

10.1002/acn3.735

Pringsheim_et_al-2019-Annals_of_Clinical_and_Translational_NeurologyLopullinen julkaistu versio, 1,28 MBLisenssi: CC BY-NC-ND

Siteeraa tätä

Pringsheim, M., Mitter, D., Schroeder, S., Warthemann, R., Pluemacher, K., Kluger, G., Baethmann, M., Bast, T., Braun, S., Buettel, H.-M., Conover, E., Courage, C., Datta, A. N., Eger, A., Grebe, T. A., Hasse-Wittmer, A., Heruth, M., Hoeft, K., Kaindl, A. M., ... Brockmann, K. (2019). Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice. Annals of Clinical and Translational Neurology, 6(4), 655-668. https://doi.org/10.1002/acn3.735

@article{457a03b7583f4763911730dbb1bd2e90,

title = "Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice",

keywords = "CONGENITAL VARIANT, CORPUS-CALLOSUM, EXPRESSION, MUTATIONS, FORNIX, OLIGODENDROCYTE, TELENCEPHALON, ASSOCIATION, MIGRATION, DISORDER, 3112 Neurosciences, 3124 Neurology and psychiatry",

author = "Milka Pringsheim and Diana Mitter and Simone Schroeder and Rita Warthemann and Kim Pluemacher and Gerhard Kluger and Martina Baethmann and Thomas Bast and Sarah Braun and Hans-Martin Buettel and Elizabeth Conover and Carolina Courage and Datta, {Alexandre N.} and Angelika Eger and Grebe, {Theresa A.} and Annette Hasse-Wittmer and Marion Heruth and Karen Hoeft and Kaindl, {Angela M.} and Stephanie Karch and Torsten Kautzky and Korenke, {Georg C.} and Bernd Kruse and Lutz, {Richard E.} and Heymut Omran and Steffi Patzer and Heike Philippi and Keri Ramsey and Tina Rating and Angelika Riess and Mareike Schimmel and Rachel Westman and Frank-Martin Zech and Birgit Zirn and Ulmke, {Pauline A.} and Godwin Sokpor and Tran Tuoc and Andreas Leha and Martin Staudt and Knut Brockmann",

year = "2019",

month = apr,

doi = "10.1002/acn3.735",

language = "English",

volume = "6",

pages = "655--668",

journal = "Annals of Clinical and Translational Neurology",

issn = "2328-9503",

publisher = "Wiley",

number = "4",

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Pringsheim, M, Mitter, D, Schroeder, S, Warthemann, R, Pluemacher, K, Kluger, G, Baethmann, M, Bast, T, Braun, S, Buettel, H-M, Conover, E, Courage, C, Datta, AN, Eger, A, Grebe, TA, Hasse-Wittmer, A, Heruth, M, Hoeft, K, Kaindl, AM, Karch, S, Kautzky, T, Korenke, GC, Kruse, B, Lutz, RE, Omran, H, Patzer, S, Philippi, H, Ramsey, K, Rating, T, Riess, A, Schimmel, M, Westman, R, Zech, F-M, Zirn, B, Ulmke, PA, Sokpor, G, Tuoc, T, Leha, A, Staudt, M & Brockmann, K 2019, 'Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice', Annals of Clinical and Translational Neurology, Vuosikerta 6, Nro 4, Sivut 655-668. https://doi.org/10.1002/acn3.735

TY - JOUR

T1 - Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice

AU - Pringsheim, Milka

AU - Mitter, Diana

AU - Schroeder, Simone

AU - Warthemann, Rita

AU - Pluemacher, Kim

AU - Kluger, Gerhard

AU - Baethmann, Martina

AU - Bast, Thomas

AU - Braun, Sarah

AU - Buettel, Hans-Martin

AU - Conover, Elizabeth

AU - Courage, Carolina

AU - Datta, Alexandre N.

AU - Eger, Angelika

AU - Grebe, Theresa A.

AU - Hasse-Wittmer, Annette

AU - Heruth, Marion

AU - Hoeft, Karen

AU - Kaindl, Angela M.

AU - Karch, Stephanie

AU - Kautzky, Torsten

AU - Korenke, Georg C.

AU - Kruse, Bernd

AU - Lutz, Richard E.

AU - Omran, Heymut

AU - Patzer, Steffi

AU - Philippi, Heike

AU - Ramsey, Keri

AU - Rating, Tina

AU - Riess, Angelika

AU - Schimmel, Mareike

AU - Westman, Rachel

AU - Zech, Frank-Martin

AU - Zirn, Birgit

AU - Ulmke, Pauline A.

AU - Sokpor, Godwin

AU - Tuoc, Tran

AU - Leha, Andreas

AU - Staudt, Martin

AU - Brockmann, Knut

PY - 2019/4

Y1 - 2019/4

KW - CONGENITAL VARIANT

KW - CORPUS-CALLOSUM

KW - EXPRESSION

KW - MUTATIONS

KW - FORNIX

KW - OLIGODENDROCYTE

KW - TELENCEPHALON

KW - ASSOCIATION

KW - MIGRATION

KW - DISORDER

KW - 3112 Neurosciences

KW - 3124 Neurology and psychiatry

U2 - 10.1002/acn3.735

DO - 10.1002/acn3.735

M3 - Article

SN - 2328-9503

VL - 6

SP - 655

EP - 668

JO - Annals of Clinical and Translational Neurology

JF - Annals of Clinical and Translational Neurology

IS - 4

ER -