Laura Hecher
Dr. med.
Laura Hecher
  • Assistant physician
Working area

Location

O47
Languages
German (Mother tongue)
English
Spanish

Areas of expertise

Publications

Zurück
  • 2024
  • 2023
  • 2022
  • 2020
  • 2019
  • 2016
  • 2014
Vor

Association between Tubulointerstitial Nephritis and Uveitis Syndrome and Small-Vessel CNS Vasculitis
Grinstein L, Hecher L, Weiss D, Johannsen J, Denecke J
NEUROPEDIATRICS. 2024;55(2):117-123.

Long-Term Antibody Response to SARS-CoV-2 in Children
Dunay G, Barroso M, Woidy M, Danecka M, Engels G, Hermann K, Neumann F, Paul K, Beime J, Escherich G, Fehse K, Grinstein L, Haniel F, Haupt L, Hecher L, Kehl T, Kemen C, Kemper M, Kobbe R, Kohl A, Klokow T, Nörz D, Olfe J, Schlenker F, Schmiesing J, Schrum J, Sibbertsen F, Stock P, Tiede S, Vettorazzi E, Zazara D, Zapf A, Lütgehetmann M, Oh J, Mir T, Muntau A, Gersting S
J CLIN IMMUNOL. 2023;43(1):46-56.

INPP4A-related genetic and phenotypic spectrum and functional relevance of subcellular targeting of INPP4A isoforms
Hecher L, Harms F, Lisfeld J, Alawi M, Denecke J, Kutsche K
NEUROGENETICS. 2023;24(2):79-93.

Specific CD4+ T Cell Responses to Ancestral SARS-CoV-2 in Children Increase With Age and Show Cross-Reactivity to Beta Variant
Paul K, Sibbertsen F, Weiskopf D, Lütgehetmann M, Barroso M, Danecka M, Glau L, Hecher L, Hermann K, Kohl A, Oh J, Wiesch J, Sette A, Tolosa E, Vettorazzi E, Woidy M, Zapf A, Zazara D, Mir T, Muntau A, Gersting S, Dunay G
FRONT IMMUNOL. 2022;13:867577.

The Clinical Picture of a Bilateral Perisylvian Syndrome as the Initial Symptom of Mega-Corpus-Callosum Syndrome due to a MAST1-Gene Mutation
Hecher L, Johannsen J, Bierhals T, Buhk J, Hempel M, Denecke J
NEUROPEDIATRICS. 2020;51(6):435-439.

Excessive Seizure Clusters in an Otherwise Well-Controlled Epilepsy as a Possible Hallmark of Untreated Vitamin B6-Responsive Epilepsy due to a Homozygous PLPBP Missense Variant
Johannsen J, Bierhals T, Deindl P, Hecher L, Hermann K, Hempel M, Kloth K, Denecke J
J PEDIATR GENET. 2019;8(4):222-225.

Dysregulation of a specific immune-related network of genes biologically defines a subset of schizophrenia
Trossbach S, Hecher L, Schafflick D, Deenen R, Popa O, Lautwein T, Tschirner S, Köhrer K, Fehsel K, Papazova I, Malchow B, Hasan A, Winterer G, Schmitt A, Meyer Zu Hörste G, Falkai P, Korth C
TRANSL PSYCHIAT. 2019;9(1):156.

Misassembly of full-length Disrupted-in-Schizophrenia 1 protein is linked to altered dopamine homeostasis and behavioral deficits
Trossbach S, Bader V, Hecher L, Pum M, Masoud S, Prikulis I, Schäble S, de Souza Silva M, Su P, Boulat B, Chwiesko C, Poschmann G, Stühler K, Lohr K, Stout K, Oskamp A, Godsave S, Müller-Schiffmann A, Bilzer T, Steiner H, Peters P, Sauvage M, Ramsey A, Miller G, Liu F, Seeman P, Brandon N, Huston J, Korth C
MOL PSYCHIATR. 2016;21(11):1561-1572.

REVERSE-TRANSLATING BIOLOGICAL MARKERS FOR DISC1-ASSOCIATED BEHAVIORAL DISORDERS TO HUMAN PATIENTS
Hecher L
2014. Schizophrenia Research - Abstracts of the 4th Biennial Schizophrenia International Research Conference. .

Letzte Aktualisierung aus dem FIS: 16.06.2024 - 04:52 Uhr