Research Explorer

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Researcher

Martin Lammens

Awards & Distinctions

13 Results

2020

Long lasting trigeminal neuropathy, limbic encephalitis and abdominal ganglionitis without primary cancer : an atypical case of Hu-Antibody syndrome

Elien De SchamphelaereAnne SiebenSebastien HeyndrickxMartin LammensKarel GeboesJan De Bleecker

A1 Journal Article in CLINICAL NEUROLOGY AND NEUROSURGERY

2019

Differences in the mitochondrial and lipid droplet morphology in female office workers with trapezius myalgia, compared to healthy controls : a muscle biopsy study

Kayleigh De MeulemeesterBarbara CagnieJo Van DorpeMartin LammensMirko PetrovicPatrick Calders

A1 Journal Article in AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION

2018

Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence

Edith BonninPauline CabochetteAlessandro FilosaRamona JühlenShoko KomatsuzakiMohammed HezwaniAchim DickmannsValérie MartinelliMarjorie VermeerschLynn Supply et al.

A1 Journal Article in PLOS GENETICS

2012

Late-onset post-irradiation vasculopathy of the posterior cerebral vasculature

Jelle van den AmeeleAnne SiebenCaroline Van den BroeckeTom BoterbergLuc DefreyneEric AchtenMartin LammensDimitri Hemelsoet

A1 Journal Article in ACTA NEUROLOGICA BELGICA

2009

Perivenous encephalomyelitis as rare cause of status epilepticus

Dimitri HemelsoetFrederic VanheeCaroline Van den BroeckeMartin LammensPaul Boon

2007

Immunohistochemical studies of oxidative phosphorylation in skeletal muscle of patients with mitochondrial tRNA gene mutations

Boel De PaepeJoél SmetMartin LammensS SENECAJ MARTINJan De BleeckerRudy Van Coster

Visualizing oxidative phosphorylation defects in skeletal muscle of patients with mitochondrial tRNA gene mutations using immunohistochemistry

Rudy Van CosterBoel De PaepeJoél SmetMartin LammensJ MARTINJan De BleeckerS SENECAW LISSENSL DE MEIRLEIR

2003

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions

IMP GOMMANSM DAVISK SAARMartin LammensF MASTAGLIAP LAMONTG VAN DUIJNHOVENHJ TER LAAKA REISOJM VOGELS et al.

A1 Journal Article in BRAIN

Development and developmental disorders of the human cerebellum

HJ TEN DONKELAARMartin LammensP WESSELINGHOM THIJSSENWO RENIER

A1 Journal Article in JOURNAL OF NEUROLOGY

Nijmegen breakage syndrome: A neuropathological study

Martin LammensJAP HIELFJM GABREELSBGM VAN ENGELENLPWJ VAN DEN HEUVELCMR WEEMAES

A1 Journal Article in NEUROPEDIATRICS

Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene

A MUCHIRBG VAN ENGELENMartin LammensJM MISLOWE MCNALLYK SCHWARTZG BONNE

A1 Journal Article in EXPERIMENTAL CELL RESEARCH

Obductie nuttig kwaliteitsinstrument vanwege onverwachte, klinisch relevante bevindingen en beantwoording van klinische vragen: een retrospectieve studie

NA van VenrooijJJWM LendersMartin LammensJHJM van Krieken

A2 Journal Article in NEDERLANDSCH TIJDSCHRIFT VOOR GENEESKUNDE

Pathogenesis of axonal dystrophy and demyelination in alpha A-crystallin-expressing transgenic mice

AF VAN RIJKMAM SWEERSGFM MERKXMartin LammensH BLOEMENDAL

A1 Journal Article in INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY