Electrophysiology - when nothing is seen

Therése Hugosson

Electrophysiology - when nothing is seen

Forskningsoutput: Avhandling › Doktorsavhandling (sammanläggning)

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Originalspråk	engelska
Kvalifikation	Doktor
Tilldelande institution	Institutionen för kliniska vetenskaper, Lund
Handledare	Englund-Johansson, Ulrica, handledare Schatz, Patrik, handledare Swanberg, Maria, handledare
Tilldelningsdatum	2018 juni 1
Utgivningsort	Lund
Förlag	Lund University: Faculty of Medicine
ISBN (tryckt)	978-91-7619-633-5
Status	Published - 2018

Bibliografisk information

Defence details
Date: 2018-06-01
Time: 13:00
Place: BMC I-1345, Sölvegatan 19 i Lund
External reviewer(s)
Name: Webster, Andrew
Title: professor
Affiliation: University College, London
---
ISSN: 1652-8220
Lund University, Faculty of Medicine Doctoral Dissertation Series 2018:67

Ämnesklassifikation (UKÄ)

Medicin och hälsovetenskap

Fria nyckelord

Elektrofysiologi
Oftalmologi

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Kappa; T HugossonPublicerad version, 587 KB

3 Artikel i vetenskaplig tidskrift

Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy.
Dalin, F., Adamus, G., Yang, S., Landgren, E., Palle, J., Hallgren, Å., Frost, B.-M., Hugosson, T., Landegren, N., Eriksson, D., Andréasson, S., Tabbara, K. F., Kämpe, O. & Alimohammadi, M., 2016, I: Ophthalmology.
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
Hugosson, T., Friedman, J. S., Ponjavic, V., Abrahamson, M., Swaroop, A. & Andréasson, S., 2010, I: Archives of Ophthalmology. 128, 6, s. 772-778
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
Friedman, J. S., Ray, J. W., Waseem, N., Johnson, K., Brooks, M. J., Hugosson, T., Breuer, D., Branham, K. E., Krauth, D. S., Bowne, S. J., Sullivan, L. S., Ponjavic, V., Gränse, L., Khanna, R., Trager, E. H., Gieser, L. M., Hughbanks-Wheaton, D., Cojocaru, R. I., Ghiasvand, N. M. & Chakarova, C. F. & 11 andra, Abrahamson, M., Goering, H. H. H., Webster, A. R., Birch, D. G., Abecasis, G. R., Fann, Y., Bhattacharya, S. S., Daiger, S. P., Heckenlively, J. R., Andréasson, S. & Swaroop, A., 2009, I: American Journal of Human Genetics. 84, 6, s. 792-800
Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

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@phdthesis{01cd1934ded443a69905019749b450b0,

title = "Electrophysiology - when nothing is seen",

keywords = "Elektrofysiologi, Oftalmologi, Electrophysiology, Ophthalmology",

author = "Ther{\'e}se Hugosson",

note = "Defence details Date: 2018-06-01 Time: 13:00 Place: BMC I-1345, S{\"o}lvegatan 19 i Lund External reviewer(s) Name: Webster, Andrew Title: professor Affiliation: University College, London --- ISSN: 1652-8220 Lund University, Faculty of Medicine Doctoral Dissertation Series 2018:67",

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isbn = "978-91-7619-633-5",

series = "Lund University, Faculty of Medicine Doctoral Dissertation Series",

publisher = "Lund University: Faculty of Medicine",

number = "67",

type = "Doctoral Thesis (compilation)",

school = "Department of Clinical Sciences, Lund",

}

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AU - Hugosson, Therése

N1 - Defence details Date: 2018-06-01 Time: 13:00 Place: BMC I-1345, Sölvegatan 19 i Lund External reviewer(s) Name: Webster, Andrew Title: professor Affiliation: University College, London --- ISSN: 1652-8220 Lund University, Faculty of Medicine Doctoral Dissertation Series 2018:67

PY - 2018

Y1 - 2018

KW - Elektrofysiologi

KW - Oftalmologi

KW - Electrophysiology

KW - Ophthalmology

M3 - Doctoral Thesis (compilation)

SN - 978-91-7619-633-5

T3 - Lund University, Faculty of Medicine Doctoral Dissertation Series

PB - Lund University: Faculty of Medicine

CY - Lund

ER -

Electrophysiology - when nothing is seen

Bibliografisk information

Ämnesklassifikation (UKÄ)

Fria nyckelord

Tillgång till dokument

Forskningsoutput

Aryl Hydrocarbon Receptor-Interacting Protein-Like 1 in Cancer-Associated Retinopathy.

Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.

Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

Citera det här