Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Habib Soua"'
Publikováno v:
Paediatrica Indonesiana, Vol 58, Iss 3, Pp 146-50 (2018)
Trisomy 13, or Patau syndrome, is a rare chromosomal disorder characterized by a triad of cleft lip and palate, postaxial polydactyly, and microphthalmia, with an incidence ranging between 1/5,000 and 1/20,000 births.1 Most patients (80%) with Patau
Externí odkaz:
https://doaj.org/article/24e077a0e68d45978de47b01941888e8
Autor:
Haifa Bouchahda, Houda El Mhabrech, Hechmi Ben Hamouda, Sobhi Ghanmi, Rim Bouchahda, Habib Soua
Publikováno v:
The Pan African Medical Journal, Vol 27, Iss 128 (2017)
The caudal regression syndrome is defined as total or partial agenesis of the sacrum and lumbar spine, frequently associated with other developmental malformations (orthopedic, neurological, genito-urinary, gastrointestinal...). Prenatal diagnosis is
Externí odkaz:
https://doaj.org/article/1eddff9257ff4e8695cd042c26fb12eb
Publikováno v:
Skinmed. 19(5)
A boy weighing 4500 g was born at 41 weeks' gestation by Cesarean section due to fetal distress. The pregnancy was complicated by gestational diabetes. He had an Apgar score of 5 and 6 after 5 and 10 minutes, respectively. At birth, the newborn manif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22691c9a4b50b55af29b7064c181505e
https://pubmed.ncbi.nlm.nih.gov/34861924
https://pubmed.ncbi.nlm.nih.gov/34861924
Publikováno v:
Paediatrica Indonesiana, Vol 58, Iss 3, Pp 146-50 (2018)
Trisomy 13, or Patau syndrome, is a rare chromosomal disorder characterized by a triad of cleft lip and palate, postaxial polydactyly, and microphthalmia, with an incidence ranging between 1/5,000 and 1/20,000 births.1 Most patients (80%) with Patau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33d76cf175ede4c2da58809269c329d7
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/1646
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/1646
Autor:
Fatma Zohra, Chioukh, Karim, Ben Ameur, Kamel, Monastiri, Hakima, Kbaier, Sonia, Blibech, Mohamed, Douagi, Khaled, Ben Hlel, Héchmi, Ben Hamouda, Habib, Soua, Amira, Bouraoui, Ridha, Régaieg, Abdellatif, Gargouri, Imène, Ksibi, Samia, Kacem, Nabiha, Mahdhaoui, Hédia, Ayech, Hassen, Sboui
Publikováno v:
La Tunisie medicale. 96(12)
To describe the transport of sick neonates to a tertiary care hospital and evaluate their condition at arrival and outcome.A multicenter, prospective cohort study was performed in 7 NICUs in Tunisia from 1st april to 31 July 2015.Demographic paramete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::341a6400519f4671e139a0fb92e97eb7
https://pubmed.ncbi.nlm.nih.gov/31131866
https://pubmed.ncbi.nlm.nih.gov/31131866
Autor:
Habib Soua, Nessrine Jammeli, Najoua Lassoued, Hechmi Ben Hammouda, Asma Wardani, Salmane Wannes, B. Mahjoub
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::768f1eda7be682e08d97456993aa433f
https://doi.org/10.1530/endoabs.63.p612
https://doi.org/10.1530/endoabs.63.p612
Autor:
Fatma Zohra, Chioukh, Karim, Ben Ameur, Nédia, Kasdallah, Sonia, Blibech, Emira, Ben Hamida, Imen, Ayadi, Héchmi, Ben Hamouda, Habib, Soua, Manel, Charfi, Nédia, Hamida, Kamel, Monastiri, Mohamed, Douagi, Zahra, Marrakchi, Abdellatif, Gargouri
Publikováno v:
La Tunisie medicale. 96(8-9)
Extremely preterm infants are newborns born before 28 weeks of gestation. Survival of these immature newborns depends on resuscitation and the quality of care during hospitalization.To determine survival and neurologic outcomes at2 years after extrem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::199b216d02f1d53a05951f321555ad38
https://pubmed.ncbi.nlm.nih.gov/30430530
https://pubmed.ncbi.nlm.nih.gov/30430530
Autor:
B. Mahjoub, Najoua Lassoued, Selmane Ouannes, Raoudha Boussoffara, Habib Soua, Mohamed Taher Sfar, Hechmi Ben Hammouda
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3d5ee144b3dde5f7083f3397045d0d7
https://doi.org/10.1530/endoabs.56.p771
https://doi.org/10.1530/endoabs.56.p771
Autor:
Habib Soua, Najoua Lassoued, Mohamed Taher Sfar, Selmen Ouannes, Raoudha Boussoffara, B. Mahjoub, Hechmi Ben Hammouda
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3af9091b43def1f8b9dcdfe7ad1f358f
https://doi.org/10.1530/endoabs.56.p772
https://doi.org/10.1530/endoabs.56.p772
Publikováno v:
The Pan African Medical Journal
The caudal regression syndrome is defined as total or partial agenesis of the sacrum and lumbar spine, frequently associated with other developmental malformations (orthopedic, neurological, genito-urinary, gastrointestinal…). Prenatal diagnosis is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8ea07bd927bd9e593a5fd8aa99a4df4
http://europepmc.org/articles/PMC5568004
http://europepmc.org/articles/PMC5568004