Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Toni Lubala Kasole"'
Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the Congo
Autor:
Daan Van Brusselen, MD, Tony Kayembe-Kitenge, MD, Sébastien Mbuyi-Musanzayi, PhD, Toni Lubala Kasole, PhD, Leon Kabamba Ngombe, PhD, Paul Musa Obadia, MD, Daniel Kyanika wa Mukoma, MSc, Koen Van Herck, ProfPhD, Dirk Avonts, ProfPhD, Koen Devriendt, ProfPhD, Erik Smolders, ProfPhD, Célestin Banza Lubaba Nkulu, ProfPhD, Benoit Nemery, ProfPhD
Publikováno v:
The Lancet Planetary Health, Vol 4, Iss 4, Pp e158-e167 (2020)
Summary: Background: Widespread environmental contamination caused by mining of copper and cobalt has led to concerns about the possible association between birth defects and exposure to several toxic metals in southern Katanga, Democratic Republic o
Externí odkaz:
https://doaj.org/article/2395c19ca5b24766b755640760b0782a
Publikováno v:
The Pan African Medical Journal, Vol 18, Iss 74 (2014)
Les auteurs rapportent un cas d'un adolescent congolais de sexe masculin, âgé de 18 ans présentant une association rare de deux maladies génétiques à savoir la drépanocytose et le diabète, afin d'inviter le monde scientifique à mettre en mar
Externí odkaz:
https://doaj.org/article/4ff65143dfea42a0ae9a92160e388634
Autor:
Sébastien Mbuyi-Musanzayi, Aimé Lumaka, Bienvenu Yogolelo Asani, Toni Lubala Kasole, Prosper Lukusa Tshilobo, Prosper Kalenga Muenze, François Tshilombo Katombe, Koenraad Devriendt
Publikováno v:
Case Reports in Genetics, Vol 2014 (2014)
Trisomy 13 is a chromosomal disorder characterized by a severe clinical picture of multiple congenital anomalies. We here describe the clinical and genetic features and prognosis observed in a newborn with trisomy 13 from Central Africa. He presented
Externí odkaz:
https://doaj.org/article/ca5e55f6f53e4ca99a2f71a58d4b8f60
Autor:
Sébastien Mbuyi-Musanzayi, Toni Lubala Kasole, Aimé Lumaka, Tony Kayembe Kitenge, Leon Kabamba Ngombe, Prosper Kalenga Muenze, Prosper Lukusa Tshilobo, François Tshilombo Katombe, Célestin Banza Lubaba Nkulu, Koenraad Devriendt
Publikováno v:
Case Reports in Genetics, Vol 2014 (2014)
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by an overgrowth, macroglossia, exomphalos, and predisposition to embryonal tumors. Central nervous abnormalities associated with BWS are rare. We describe a one-day-old Co
Externí odkaz:
https://doaj.org/article/154dbb25c7f74345913e9cff73dff4b5
Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the Congo
Autor:
Koen Van Herck, Erik Smolders, Toni Lubala Kasole, Célestin Banza Lubaba Nkulu, Léon Kabamba Ngombe, Benoit Nemery, Tony Kayembe-Kitenge, Paul Musa Obadia, Dirk Avonts, Daan Van Brusselen, Koen Devriendt, Daniel Kyanika wa Mukoma, Sébastien Mbuyi-Musanzayi
Publikováno v:
LANCET PLANETARY HEALTH
The Lancet Planetary Health, Vol 4, Iss 4, Pp e158-e167 (2020)
The Lancet Planetary Health, Vol 4, Iss 4, Pp e158-e167 (2020)
BACKGROUND: Widespread environmental contamination caused by mining of copper and cobalt has led to concerns about the possible association between birth defects and exposure to several toxic metals in southern Katanga, Democratic Republic of the Con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc01c2fed23c305590b9ee91f2e1ec82
https://lirias.kuleuven.be/handle/123456789/654307
https://lirias.kuleuven.be/handle/123456789/654307
Autor:
François Tshilombo Katombe, Prosper Lukusa Tshilobo, Toni Lubala Kasole, Bienvenu Yogolelo Asani, Aimé Lumaka, Koenraad Devriendt, Prosper Kalenga Muenze, Hervé Reychler, Sébastien Mbuyi-Musanzayi, Erick Kasamba Ilunga
Wolf-Hirschhorn syndrome (WHS) is a multiple congenital anomaly-intellectual disability syndrome caused by a deletion involving chromosome 4p16.3. We report clinical and genetic findings of the first WHS patient diagnosed in central Africa. This boy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36efcd8f8df256c6ae448396a0e0c235
https://europepmc.org/articles/PMC5548528/
https://europepmc.org/articles/PMC5548528/
Autor:
Léon Kabamba Ngombe, Prosper Lukusa Tshilobo, Sébastien Mbuyi-Musanzayi, François Tshilombo Katombe, Koenraad Devriendt, Toni Lubala Kasole, Prosper Kalenga Muenze, Tony Kayembe Kitenge
Publikováno v:
Clinical Dysmorphology. 24:173-175
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9841b0257d3f451724008cae5bd6706
https://doi.org/10.1097/mcd.0000000000000086
https://doi.org/10.1097/mcd.0000000000000086
Publikováno v:
The Pan African Medical Journal
Les auteurs rapportent un cas d'un adolescent congolais de sexe masculin, âgé de 18 ans présentant une association rare de deux maladies génétiques à savoir la drépanocytose et le diabète, afin d'inviter le monde scientifique à mettre en mar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b37b4af8e006ea4c9d392bf951298ba6
https://pubmed.ncbi.nlm.nih.gov/25400841
https://pubmed.ncbi.nlm.nih.gov/25400841
Publikováno v:
The Pan African Medical Journal, Vol 18, Iss 74 (2014)
Les auteurs rapportent un cas d'un adolescent congolais de sexe masculin, âge de 18 ans presentant une association rare de deux maladies genetiques a savoir la drepanocytose et le diabete, afin d'inviter le monde scientifique a mettre en marche des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23812e5aa65a5adf7a0ef1a9985e2add
https://doaj.org/article/4ff65143dfea42a0ae9a92160e388634
https://doaj.org/article/4ff65143dfea42a0ae9a92160e388634
Autor:
Tony Kayembe Kitenge, Léon Kabamba Ngombe, Sébastien Mbuyi-Musanzayi, Prosper Kalenga Muenze, François Tshilombo Katombe, Aimé Lumaka, Koenraad Devriendt, Célestin Banza Lubaba Nkulu, Prosper Lukusa Tshilobo, Toni Lubala Kasole
Publikováno v:
Case Reports in Genetics, Vol 2014 (2014)
Case Reports in Genetics
Case Reports in Genetics
Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome characterized by an overgrowth, macroglossia, exomphalos, and predisposition to embryonal tumors. Central nervous abnormalities associated with BWS are rare. We describe a one-day-old Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::498674643e5fbd6bc2cc2feefda444e5
https://lirias.kuleuven.be/handle/123456789/481839
https://lirias.kuleuven.be/handle/123456789/481839