Ghent University Academic Bibliography

Show Sort by

Your filters: cql: author="D'Hooghe, Marc" or (type exact bookEditor and editor="D'Hooghe, Marc")

Add to list
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Jennelle C Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M Seabra, Mary-Alice Abbott, et al.

(2017) NATURE GENETICS. 49(1). p.36-45
Add to list
- Conference Paper
- C3
Development of an S-G2 micronucleus assay for the detection of in vitro chromosomal radiosensitivity in high-risk women subjected to early mammography screening for breast cancer

Anne Vral (UGent) , Julie Depuydt (UGent) , Annelot Baert (UGent) , Bruce Poppe (UGent) , Tom Van Maerken (UGent) , Fransiska Malfait (UGent) , Kim De Leeneer (UGent) , Marc D'Hooghe and Kathleen Claes (UGent)

(2013) INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE. 32(suppl. 1). p.S51-S51
Add to list
Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives

Kathleen Claes (UGent) , Julie Depuydt (UGent) , A Malcolm R Taylor, James I Last, Annelot Baert (UGent) , Peter Schietecatte (UGent) , Veerle Vandersickel (UGent) , Bruce Poppe (UGent) , Kim De Leeneer (UGent) , Marc D'Hooghe, et al.

(2013) NEUROMOLECULAR MEDICINE. 15(3). p.447-457
Add to list
X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutation

Marc D'Hooghe, Dominik Selleslag, Geert Mortier, Rudy Van Coster (UGent) , Pieter Vermeersch, Johan Billiet and Soumeya Bekri

(2012) EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 16(6). p.730-735
Add to list
Steroids in intractable childhood epilepsy: clinical experience and review of the literature

Helene Verhelst (UGent) , Paul Boon (UGent) , Gunnar Buyse, Berten Ceulemans, Marc D'Hooghe, Linda De Meirleir, Danièle Hasaerts, An Jansen, Lieven Lagae, Alfred Meurs (UGent) , et al.

(2005) SEIZURE-EUROPEAN JOURNAL OF EPILEPSY. 14(6). p.412-421
Add to list
- Conference Paper
- C3
- open access
Differential organ involvement in peroxisomal disorders

Frank Roels (UGent) , Marianne Depreter, Marisa Giros, Sylvia Stockler, Hannah Mandel, D Troost, Boel De Paepe (UGent) , Jan De Bleecker (UGent) , Marc D'Hooghe, Christian Nuttin, et al.

(2002) JOURNAL OF INHERITED METABOLIC DISEASE. 25(suppl. 1). p.99-99

Academic Bibliography

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Development of an S-G2 micronucleus assay for the detection of in vitro chromosomal radiosensitivity in high-risk women subjected to early mammography screening for breast cancer

Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives

X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutation

Steroids in intractable childhood epilepsy: clinical experience and review of the literature

Differential organ involvement in peroxisomal disorders

Contents

Support

Contact