Martin M Y Lammens (Martin Lammens)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 11

Top Venues

American journal of medical genetics. Part A

Histochemistry and cell biology

Genetics in medicine : official journal of the American College of Medical Genetics

Acta neurologica Belgica

Antwerp University Hospital

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Antwerp University Hospital Nov 01 2012

Belgium

Chief :: Pathology

Radboud University Nijmegen Medical Centre Aug 01 1999 - Oct 31 2012

Netherlands

Staff member :: Pathology

Publications

Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Kan Yan Chloe Li, Hector Dejea, Koen De Winne, Anne Bonnin, Valentino D'Onofrio, Janneke A Cox, Patricia Garcia-Canadilla, Martin M Y Lammens, Andrew C Cook, Álvaro Sepúlveda-Martínez, Amélie Dendooven
Feasibility and safety of synchrotron-based X-ray phase contrast imaging as a technique complementary to histopathology analysis. Histochemistry and cell biology (2023)
Lina Daoud, Idil Gunes Tatar, Christian Raftopoulos, Martin M Y Lammens
Intermediate grade meningeal melanocytoma of the posterior fossa, GNAQ mutation-positive. Acta neurologica Belgica (2023)
An Hotterbeekx, Martin M Y Lammens, Sylvester Onzivua, Robert Lukande, Francis Olwa, Samir Kumar-Singh, Stijn Van Hees, Richard Idro, Robert Colebunders
Neuropathological Changes in Nakalanga Syndrome-A Case Report. Pathogens (Basel, Switzerland) 10 (2) (2021)
Jeroen Kerstens, Busra Durmus, Stijn Lambrecht, Ingrid Baar, Margareta M Ieven, Thijs van der Zijden, Paul M Parizel, Tomas Menovsky, Martin M Y Lammens, Philippe G Jorens
Meningoencephalitis with Streptococcus equi Subspecies equi Leading to a Dural Arteriovenous Fistula. Case reports in neurological medicine 2021 (2021)
Peter A van Dam, Yannick Verhoeven, Julie Jacobs, An Wouters, Wiebren Tjalma, Filip Lardon, Tim Van den Wyngaert, Jonatan Dewulf, Evelien L J Smits, Cécile Colpaert, Hans Prenen, Marc Peeters, Martin M Y Lammens, Xuan Bich Trinh
RANK-RANKL Signaling in Cancer of the Uterine Cervix: A Review. International journal of molecular sciences 20 (9) (2019)
Josephina A N Meester, Geert Vandeweyer, Isabel Pintelon, Martin M Y Lammens, Lana Van Hoorick, Simon De Belder, Kathryn Waitzman, Luciana Young, Larry W Markham, Julie Vogt, Julie Richer, Luc M Beauchesne, Sheila Unger, Andrea Superti-Furga, Milan Prsa, Rami Dhillon, Edwin Reyniers, Harry C Dietz, Wim Wuyts, Geert Mortier, Aline Verstraeten, Lut Van Laer, Bart L Loeys
Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Martin M Y Lammens (Martin Lammens)