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Inhibition of human placental endothelial cell proliferation and angiogenesis by netrin-4

Autor: S. Si Nacer, Wael Traboulsi, Jean-Jacques Feige, Sophie Brouillet, P. De Mazancourt, Nadia Alfaidy, M. Dakouane-Giudicelli, M. Vallée, G. Vallat, A. Torre

Publikováno v: Placenta
Placenta, Elsevier, 2015, 36 (11), pp.1260-1265. ⟨10.1016/j.placenta.2015.09.007⟩
Placenta, 2015, 36 (11), pp.1260-1265. ⟨10.1016/j.placenta.2015.09.007⟩

Introduction Netrin-4 is a secreted member of the laminin-related protein family, known to be involved in axonal guidance and endothelial cell survival, proliferation, and migration. We have recently reported the cellular localization of netrin-4 and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9debf0719f4c1a23ffca35901c160a4
https://hal.archives-ouvertes.fr/hal-02385077

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Profil electroneuromyographique des neuropathies dans une population de patients diabetiques admis dans un laboratoire de neurophysiologie

Autor: G Gallouedec, D Gnonlonfoun, M Khalil, G Vallat, L Magy, A Adoukonou

Publikováno v: African Journal of Neurological Sciences; Vol 27, No 2 (2008)

Les neuropathies peripheriques constituent une complication frequente du diabete. Plusieurs formes de neuropathies sont decrites dans cette population. L’objectif de ce travail etait d’etudier la frequence des differentes neuropathies dans une po

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fca7b92c95fc14e96ec7ec6db9627c0
https://www.ajol.info/index.php/ajns/article/view/55102

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Conference

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Akademický článek

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[Hereditary osteo-onychodysplasia. Histomorphometric bone study. Apropos of a case]

Autor: J F, Rossi, D, Kha Tu, P, Baldet, A, Dubois, M, Brunel, C, Janbon, G, Vallat

Publikováno v: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 59(6)

The authors report on a patient with hereditary osteo-onychodysplasia (HOOD). Osteoporosis was demonstrated upon histomorphologic bone examination. HOOD is a rare inherited disorder. Typical features include dysplasia of the nails, patellae, elbows a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::36dee5ac0f74294773e56bb5a44e314e
https://pubmed.ncbi.nlm.nih.gov/6302877

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[Renal manifestations in Hodgkin disease. Two case-reports with a review of the medical literature (author's transl)]

Autor: J F, Rossi, A, Dubois, M, Brunel, C, Janbon, G, Vallat

Publikováno v: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 58(24)

The authors report on two patients in whom Hodgkin disease was revealed by renal complications: nephrotic syndrome in one patient and renal failure with enlarged kidneys secondary to malignant infiltration in the other. In comparison to other lymphom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::97b69ccfea564389df1e77fc9624f1a1
https://pubmed.ncbi.nlm.nih.gov/6287613

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[Role of gamma cineangiography in the evaluation of chronic cerebral arteriopathies]

Autor: J L, Hirsch, J, Chevalier, G, Vallat

Publikováno v: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 59(40)

Gamma scintigraphy plays an important role in the topographic diagnosis of focalized cerebrovascular insufficiency. Furthermore, sequential imaging allows a comparative study of arterial distribution while studying the "transit time" of the radioacti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::88fd9eb7ec04b5cd2a1b3414ac93b8bf
https://pubmed.ncbi.nlm.nih.gov/6316540

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[Prolymphocytic leukemia of T-cell type. Clinical, cytological, cytochemical and immunological studies (author's transl)]

Autor: J L, Richard, J F, Vives, J, Clot, J, Taib, M F, Lambert, C, Janbon, G, Vallat

Publikováno v: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 57(29-32)

Prolymphocytic leukaemia (PL) is a rare variant of lympho-proliferative disorder, defined by Galton [21], which differs clearly from CLL by clinical, haematological and immunological features. Nevertheless like CLL, PL appears to represent predominan

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f55caea1b68b2f5e13df23607fb4a27e
https://pubmed.ncbi.nlm.nih.gov/6269211

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