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Loeys, Bart
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Search Results - Loeys, Bart
Showing
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Loeys, Bart
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1
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome
by
Valdivia Callejon, Irene
,
Buccioli, Lucia
,
Bastianen, Jarl
,
Schippers, Jolien
,
Verstraeten, Aline
,
Luyckx, Ilse
,
Peeters, Silke
,
Danser, A H Jan
,
Van Kimmenade, Roland R J
,
Meester, Josephina
,
Loeys, Bart
Published in
International journal of molecular sciences
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2
FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature
by
Cannaerts, Elyssa
,
Shukla, Anju
,
Hasanhodzic, Mensuda
,
Alaerts, Maaike
,
Schepers, Dorien
,
Van Laer, Lut
,
Girisha, Katta M
,
Hojsak, Iva
,
Loeys, Bart
,
Verstraeten, Aline
Published in
BMC medical genetics
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3
Defining the Clinical, Molecular and Ultrastructural Characteristics in Occipital Horn Syndrome: Two New Cases and Review of the Literature
by
Beyens, Aude
,
Van Meensel, Kyaran
,
Pottie, Lore
,
De Rycke, Riet
,
De Bruyne, Michiel
,
Baeke, Femke
,
Hoebeke, Piet
,
Plasschaert, Frank
,
Loeys, Bart
,
De Schepper, Sofie
,
Symoens, Sofie
,
Callewaert, Bert
Published in
Genes
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4
First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report
by
Baban, Anwar
,
Magliozzi, Monia
,
Loeys, Bart
,
Adorisio, Rachele
,
Alesi, Viola
,
Secinaro, Aurelio
,
Corica, Bernadette
,
Vricella, Luca
,
Dietz, Harry C
,
Drago, Fabrizio
,
Novelli, Antonio
,
Amodeo, Antonio
Published in
BMC medical genetics
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5
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease
by
Preuss, Christoph
,
Capredon, Melanie
,
Wünnemann, Florian
,
Chetaille, Philippe
,
Prince, Andrea
,
Godard, Beatrice
,
Leclerc, Severine
,
Sobreira, Nara
,
Ling, Hua
,
Awadalla, Philip
,
Thibeault, Maryse
,
Khairy, Paul
,
Samuels, Mark E
,
Andelfinger, Gregor
Published in
PLoS genetics
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6
Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients
by
ZHURAYEV, RUSTAM
,
PROOST, DORIEN
,
ZERBINO, DMYTRO
,
FEDORENKO, VIKTOR
,
MEESTER, JOSEPHINA A. N.
,
VAN LAER, LUT
,
LOEYS, BART L.
Published in
Genetics Research
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7
Heritable Connective Tissue Disorders in Childhood: Increased Fatigue, Pain, Disability and Decreased General Health
by
Warnink-Kavelaars, Jessica
,
de Koning, Lisanne E
,
Rombaut, Lies
,
Alsem, Mattijs W
,
Menke, Leonie A
,
Oosterlaan, Jaap
,
Buizer, Annemieke I
,
Engelbert, Raoul H H
,
On Behalf Of The Pediatric Heritable Connective Tissue Disorders Study Group
Published in
Genes
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Genetics & Heredity
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Marfan Syndrome
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Mutation
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Young Adult
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Adolescent
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Connective Tissue Diseases
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Child, Preschool
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Aneurysms
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