Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Molla Taye"'
Autor:
Assefa Agegnehu Teshome, Gashaw Walle Ayehu, Berhanu Kindu Ashagrie, Nega Dagnaw Baye, Atalo Agemas Ayenew, Misganaw Asmamaw Mengstie, Taklo Simeneh Yazie, Asaye Alamneh Gebeyehu, Ermias Sisay Chanie, Yalew Melkamu Molla, Molla Taye Jemberie, Agmas Wassie Abate
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
PurposeThe purpose of this systematic review is to answer the focused question, “What is the commonly affected nerve branch and the side of the face involved in trigeminal neuralgia?”Types of studies reviewedThis systematic review included studie
Externí odkaz:
https://doaj.org/article/b335dbff0938428d9be795d6e8e8d6bd
Publikováno v:
Health Services Insights, Vol 14 (2021)
This study aimed to assess maternal satisfaction and associated factors with delivery care services uptake among mothers who gave birth at public health centers. An institution-based cross-sectional study was conducted in the Yeka Sub-City in Addis A
Externí odkaz:
https://doaj.org/article/937b2b724f924df291b89d2e870d0313
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-11 (2019)
Abstract Background During the first three months of pregnancy, the developing embryo may be susceptible to external and internal factors, which may lead to structural and functional congenital anomalies. The main objective of this study was to deter
Externí odkaz:
https://doaj.org/article/8a68120fce1b4c6187b826025825e13a
Autor:
Molla Taye
Publikováno v:
PLoS ONE, Vol 16, Iss 11 (2021)
Introduction Knowledge and beliefs of people on congenital malformations and their causes differ from society to society. As a result, there is a paucity of understanding community perceived knowledge and beliefs towards congenital malformations and
Externí odkaz:
https://doaj.org/article/cd78a72f05f94cf8bf39b57a9bec8db1
Publikováno v:
Scientifica, Vol 2020 (2020)
Spina bifida is an abnormal closure of the neural tube during the fourth week of development. It is the major cause of fetal loss and considerable disabilities in newborns. The aim of this review is to determine the pooled prevalence of spina bifida
Externí odkaz:
https://doaj.org/article/3cedc2528a284b7783a76766fc7f5569
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-11 (2018)
Abstract Background The early stage of embryo development is extremely vulnerable to various teratogenic factors, leading to congenital anomalies. In Ethiopia, a significant number of babies are born with congenital anomalies, but the risk factors fo
Externí odkaz:
https://doaj.org/article/bc86f0d9e1fc44ef8903ce8fe28f6fe7
Publikováno v:
International Journal of Anatomy Radiology and Surgery, Vol 5, Iss 4, Pp AO01-AO07 (2016)
Introduction: Human palmar digital dermatoglyphic patterns are individually unique and permanent throughout life. Patterns of skin ridge lines of ink are used in forensic science and have diagnostic value in clinical and genetical abnormalities.
Externí odkaz:
https://doaj.org/article/03405220e36b4bdb832853c300086651
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0161998 (2016)
BACKGROUND:Birth defects are defined as structural and functional defects that develop during the organogenesis period and present at birth or detected later in life. They are one of the leading causes of infant and child mortality, morbidity, and lo
Externí odkaz:
https://doaj.org/article/0fdc916a85bb42a5be783c561dd8fb38
Autor:
Teshome, Assefa Agegnehu, Ayehu, Gashaw Walle, Ashagrie, Berhanu Kindu, Baye, Nega Dagnaw, Ayenew, Atalo Agemas, Mengstie, Misganaw Asmamaw, Yazie, Taklo Simeneh, Gebeyehu, Asaye Alamneh, Chanie, Ermias Sisay, Molla, Yalew Melkamu, Jemberie, Molla Taye, Abate, Agmas Wassie
Publikováno v:
Frontiers in Neurology; 2024, p1-7, 7p
Autor:
Daniel Gashaneh Belay, Misganaw Gebrie Worku, Meselech Ambaw Dessie, Yared Asmare, Molla Taye
Publikováno v:
Anatomy & Cell Biology. 55:161-169
Palmar creases are unique, permanent, and genetically controlled morphological variables. Recognizing palmar crease types are important for personal identification, criminal investigations, and diagnosis of congenital diseases. This study aimed to re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e27d200162928af55338fab119c4b82
https://doi.org/10.5115/acb.21.251
https://doi.org/10.5115/acb.21.251