Ghent University Academic Bibliography

Your filters: cql: author="MARTIN, J" or (type any "bookEditor issueEditor" and editor="MARTIN, J")

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Extended pharmacological thromboprophylaxis and clinically relevant venous thromboembolism after major abdominal and pelvic surgery : international, prospective, propensity score-weighted cohort study

A Sgrò, R Blanco-Colino, N Brindl, D Chaudhry, K Gressmann, R R Gujjuri, A Hilder, E Matey, I S Pereira, A Turňa, et al.

(2025) BJS-BRITISH JOURNAL OF SURGERY. 112(3).
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Machine learning risk prediction of mortality for patients undergoing surgery with perioperative SARS-CoV-2 : the COVIDSurg mortality score

[missing] COVIDSurg Collaborative, I Dajti, J I Valenzuela, L A Boccalatte, N A Gemelli, D E Smith, N N Dudi-Venkata, H M Kroon, T Sammour, M Roberts, et al.

(2021) BRITISH JOURNAL OF SURGERY. 108(11). p.1274-1292
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Epithelial dysregulation in obese severe asthmatics with gastro-oesophageal reflux

Jeanne-Marie Perotin, James PR Schofield, Susan J Wilson, Jonathan Ward, Joost Brandsma, Fabio Strazzeri, Aruna Bansal, Xian Yang, Anthony Rowe, Julie Corfield, et al.

(2019) EUROPEAN RESPIRATORY JOURNAL. 53(6).
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High loading of polygenic risk for ADHD in children with comorbid aggression

ML Hamshere, K Langley, J Martin, SS Agha, E Stergiakouli, RJL Anney, J Buitelaar, SV Faraone, KP Lesch, BM Neale, et al.

(2013) AMERICAN JOURNAL OF PSYCHIATRY. 170(8). p.909-916
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- Conference Paper
- C3
The cure of the 'Berlin patient': why did pre-existing X4-variants not emergence after allogeneic CCR5-Delta 32 SCT?

J Symons, S Deeks, G Hutter, A Wensing, J Martin, P van Ham, Linos Vandekerckhove (UGent) and M Nijhuis

(2012) JOURNAL OF THE INTERNATIONAL AIDS SOCIETY. 15(suppl. 3). p.17-18
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Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

L Diaz-Gallo, P Gourh, J Broen, C Simeon, V Fonollosa, N Ortego-Centeno, S Agarwal, MC Vonk, M Coenen, G Riemekasten, et al.

(2011) ANNALS OF THE RHEUMATIC DISEASES. 70(3). p.454-462
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- Conference Paper
- C3
Immunohistochemical studies of oxidative phosphorylation in skeletal muscle of patients with mitochondrial tRNA gene mutations

Boel De Paepe (UGent) , Joél Smet (UGent) , Martin Lammens (UGent) , S SENECA, J MARTIN, Jan De Bleecker (UGent) and Rudy Van Coster (UGent)

(2007) NEUROMUSCULAR DISORDERS. 17. p.767-768
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- Conference Paper
- C3
Visualizing oxidative phosphorylation defects in skeletal muscle of patients with mitochondrial tRNA gene mutations using immunohistochemistry

Rudy Van Coster (UGent) , Boel De Paepe (UGent) , Joél Smet (UGent) , Martin Lammens (UGent) , J MARTIN, Jan De Bleecker (UGent) , S SENECA, W LISSENS and L DE MEIRLEIR

(2007) JOURNAL OF INHERITED METABOLIC DISEASE. 30 : Suppl. 1. p.72-72
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- Journal Article
- A2
Infantile presentation of the mitochondrial A8344G mutation.

E SCALAIS, C NUTTIN, S SENECA, Joél Smet (UGent) , Boel De Paepe (UGent) , J MARTIN, R STEVENS, F PIERART, O BATTISTI, W LISSENS, et al.

(2007) European journal of neurology. 11. p.3-5
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Feasibility assessment of a sedation delivery system to administer propofol for GI endoscopy

ANNELIESE MOERMAN, D PAMBIANCO, J RORIE, J MARTIN and Michel Struys (UGent)

(2006) Asa Annual Meetings 2006.

Academic Bibliography

Extended pharmacological thromboprophylaxis and clinically relevant venous thromboembolism after major abdominal and pelvic surgery : international, prospective, propensity score-weighted cohort study

Machine learning risk prediction of mortality for patients undergoing surgery with perioperative SARS-CoV-2 : the COVIDSurg mortality score

Epithelial dysregulation in obese severe asthmatics with gastro-oesophageal reflux

High loading of polygenic risk for ADHD in children with comorbid aggression

The cure of the 'Berlin patient': why did pre-existing X4-variants not emergence after allogeneic CCR5-Delta 32 SCT?

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

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

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

Infantile presentation of the mitochondrial A8344G mutation.

Feasibility assessment of a sedation delivery system to administer propofol for GI endoscopy

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