Results 91 to 100 of about 1,837 (195)

Genetics and Genetic Testing in Congenital Heart Disease [PDF]

, 2015
Congenital heart defects (CHDs) are structural abnormalities of the heart and great vessels that are present from birth. The presence or absence of extra-cardiac anomalies has historically been used to identify patients with possible monogenic ...
Cowan, Jason R., Ware, Stephanie M.
core   +1 more source

Dentoalveolar heights in skeletal class I normodivergent facial patterns [PDF]

, 2012
OBJECTIVE: To determine the dentoalveolar heights (mm) in skeletal class I normodivergent facial pattern and compare the same heights in male and female subjects. STUDY DESIGN: Cross-sectional observational study.
Fida, Mubassar, Shaikh, Attiya, Zafar-Ul-Islam,   +2 more
core   +1 more source

International Veterinary Epilepsy Task Force recommendations for systematic sampling and processing of brains from epileptic dogs and cats [PDF]

, 2015
Traditionally, histological investigations of the epileptic brain are required to identify epileptogenic brain lesions, to evaluate the impact of seizure activity, to search for mechanisms of drug-resistance and to look for comorbidities.
A Jeans, A Katelaris, A Klang, A Pakozdy, A Pakozdy, A Pitkanen, A Woznicka, Akos Pakozdy, AM Wahle, Andrea Fischer, Andrea Tipold, Clare Rusbridge, DM Kowalska, Edward E. Patterson, ES Park, Eva Wagner, F Reinoso-Suárez, Francisco Fernández-Flores, G Isoardo, H Potschka, H Urbach, Heidrun Potschka, HO Lüders, Holger A. Volk, I Blumcke, I Toyoda, IK Hwang, J O’Muircheartaigh, Jacques Penderis, JE Cavazos, JH Margerison, JN Kornegay, JY Cheong, K Baiker, K Kobow, Karen Muñana, Kaspar Matiasek, L Wang, LP Hudson, Luisa De Risio, M Fischer, M Manford, M Oehmichen, M Sasaki, M Singer, M Thom, M Thom, M Wolf, Marco Rosati, Martí Pumarola i Batlle, ME Milne, Mette Berendt, Michael Podell, MP Witter, N Shihab, PS Buckmaster, R Adamec, R Crooks, RE Adamec, RE Adamec, RM Packer, RN Auer, Robyn G. Farquhar, S Lomoio, S Schriefl, Sam Long, Simon Platt, Sofie F. M. Bhatti, SY Bando, T Kuwabara, TS Jokinen, U Seneviratne, VA Gil, Veronika M. Stein, Y Masuo, Z Ahmed   +75 more
core   +7 more sources

Anatomical landmarks for transnasal endoscopic skull base surgery [PDF]

, 2018
Resection of midline skull base lesions involve approaches needing extensive neurovascular manipulation. Transnasal endoscopic approach (TEA) is minimally invasive and ideal for certain selected lesions of the anterior skull base. A thorough knowledge of
Monnier, Philippe, Pasche, Philippe, Sandu, Kishore   +2 more
core  

Frontonasal dysplasia Sequence : A case report

Nigerian Journal of Paediatrics
Frontonasal dysplasia (FND) is a very rare congenital abnormality in which the mid face does not develop normally. It affects mainly the head and face. Cause is unknown but may be sporadic or familial.
Bello M , Garandawa H, Mustapha Z, Isa A, Tahir C, Ngamdu YB, Machoko Y, Abubakar H, Djossi SK   +8 more
doaj  

Olfactory Deficits In Cleft Lip And Palate [PDF]

, 2011
Cleft lip with or without an associated cleft palate (CL/P) is one of the most common congenital birth defects. Both the frequency with which it occurs and the high psychosocial and financial costs associated with CL/P contribute to a significant public ...
May, Maureen A
core  

Surgical Management of a Mild Case of Frontonasal Dysplasia: A Case Report and Review of Literature. [PDF]

Cureus, 2021
Ainuz BY, Wolfe EM, Wolfe SA.
europepmc   +1 more source

Frontofacionasal dysplasia: another observation [PDF]

, 2009
Frontofacionasal dysplasia (FFND) is a rare group of disorders, characterized by ocular hypertelorism and frontonasal process anomalies in which clinical and etiological heterogeneity have been recognized since the first review by Gollop 1981.1 ...
Sadik, DI, Shawky, RM
core   +1 more source

Frontonasal dysplasia [PDF]

, 2020
openaire   +3 more sources

The Syndrome of Frontonasal Dysplasia, Callosal Agenesis, Basal Encephalocele, and Eye Anomalies – Phenotypic and Aetiological Considerations

International Journal of Medical Sciences, 2004
We report ten sporadic cases of Brazilian patients with facial midline defects, callosal agenesis, basal encephalocele, and ocular anomalies. This very rare cluster of anomalies has been well reported before. However, only until recently it is recognized
doaj