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pro vyhledávání: '"Melek Ahmed"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Key Clinical Message Myeloma of the thyroid cartilage is a rare but important differential diagnosis of a laryngeal mass. Although hoarseness as the initial presenting symptom in multiple myeloma is extremely rare, a clinician should always consider
Externí odkaz:
https://doaj.org/article/c7483969a6864c49b457e99c51a859d3
Autor:
Melek Ahmed, Mania De Praeter, Joris Verlooy, An-Sofie Schoonjans, Sven Dekeyzer, Stephanie Vanden Bossche, Martin Lammens, Patrick Pauwels
Publikováno v:
Clinical neuropathology
Autor:
Melek Ahmed, Barbara Verbraeken, Tomas Menovsky, Vincent Van Rompaey, Krystyna Szewczyk, Martin Lammens, Christophe Hermans
Publikováno v:
Nanomedicine: nanotechnology, biology and medicine
There is a continued need for effective hemostatic agents that are safe for neurosurgical use. Self-assembling peptide hydrogels have been suggested as novel hemostatic agents. They offer some advantages for neurosurgical hemostasis (e.g., transparen
Autor:
Amélie Dendooven, Glenn Broeckx, Amaryllis H. Van Craenenbroeck, Karin Schildermans, Melek Ahmed, Geert Baggerman, Patrick Pauwels
Publikováno v:
Journal of clinical pathology
Traditionally, immunohistochemistry (IHC) is used by pathologists to localise specific proteins or peptides in tissue slides. In the era of personalised medicine, however, molecular tissue analysis becomes indispensable for correct diagnosis, prognos
Autor:
Martin Lammens, Hilde Van Esch, Anne Rochtus, Gillian I. Rice, Paul De Cock, Chiara De Luca, Mathieu P Rodero, Melek Ahmed, Lieven Lagae, Yanick J. Crow
Publikováno v:
Clinical Genetics
Clinical Genetics, Wiley, 2020, 98 (5), pp.423-432. ⟨10.1111/CGE.13761⟩
De Luca, C, Crow, Y J, Rodero, M, Rice, G I, Ahmed, M, Lammens, M, De Cock, P, Van Esch, H, Lagae, L & Rochtus, A 2020, ' Expanding the clinical spectrum of Fowler syndrome : Three siblings with survival into adulthood and systematic review of the literature ', Clinical Genetics . https://doi.org/10.1111/cge.13761
Clinical genetics
Clinical Genetics, Wiley, 2020, 98 (5), pp.423-432. ⟨10.1111/CGE.13761⟩
De Luca, C, Crow, Y J, Rodero, M, Rice, G I, Ahmed, M, Lammens, M, De Cock, P, Van Esch, H, Lagae, L & Rochtus, A 2020, ' Expanding the clinical spectrum of Fowler syndrome : Three siblings with survival into adulthood and systematic review of the literature ', Clinical Genetics . https://doi.org/10.1111/cge.13761
Clinical genetics
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (PVHH, OMIM 225790), also known as Fowler syndrome, is a rare autosomal recessive disorder of brain angiogenesis. PVHH has long been considered to be prenatally lethal. We evaluated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda6d81ef972a6ddd0ff32cd7e256ba6
https://hal.archives-ouvertes.fr/hal-02996391
https://hal.archives-ouvertes.fr/hal-02996391
Autor:
Martin Lammens, Lieven Lagae, Melek Ahmed, Hilde Van Esch, Mathieu P Rodero, Gillian I. Rice, Anne Rochtus, Paul De Cock, Chiara De Luca, Yanick J. Crow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3417163e4f9f7808c09fdee6ce82cec
https://doi.org/10.1111/cge.13761/v2/response1
https://doi.org/10.1111/cge.13761/v2/response1