Results 11 to 20 of about 79,532 (296)

Supernumerary Tooth Patterns in Non-Syndromic White European Subjects [PDF]

Dentistry Journal, 2023
Supernumerary teeth form at an incidence of about 3% in the population, with differences among races and various clinical consequences. Information on detailed patterns, and especially on white subjects, is scarce in the literature.
Eva Henninger, Luca Friedli, Miltiadis A. Makrygiannakis, Vasileios F. Zymperdikas, Moschos A. Papadopoulos, Georgios Kanavakis, Nikolaos Gkantidis   +6 more
doaj   +3 more sources

Genetic insights into non-syndromic Tetralogy of Fallot [PDF]

Frontiers in Physiology, 2022
Congenital heart defects (CHD) include structural abnormalities of the heart or/and great vessels that are present at birth. CHD affects around 1% of all newborns worldwide.
Nouf J. Althali, Nouf J. Althali, Kathryn E. Hentges   +2 more
doaj   +2 more sources

RETRACTED: Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis. [PDF]

PLoS ONE, 2016
Recent studies have demonstrated that ectodysplasin-A (EDA) mutations are associated with non-syndromic tooth agenesis. Indeed, we were the first to report three novel EDA mutations (A259E, R289C and R334H) in sporadic non-syndromic tooth agenesis.
Wenjing Shen, Yue Wang, Yang Liu, Haochen Liu, Hongshan Zhao, Guozhong Zhang, Malcolm L Snead, Dong Han, Hailan Feng   +8 more
doaj   +2 more sources

Non-Syndromic Spinal Schwannomas: A Novel Classification [PDF]

Frontiers in Neurology, 2017
Schwannomas are the most frequent primary tumors of the spine with an incidence of 0.3-0.5/100,000 person per year. Current treatment for non-syndromic spinal schwannomas is total resection of the tumor with preservation of neurovascular structures. This study aims to report neurologic and radiologic outcome following treatment of non-syndromic spinal ...
Sun, Ibrahim, Pamir, M. Necmettin
openaire   +6 more sources

Genetic analysis of non‐syndromic craniosynostosis [PDF]

Orthodontics & Craniofacial Research, 2007
Structured AbstractAuthors –  Simeon A. BoyadjievCraniosynostosis is a common malformation occurring in 3–5 per 10 000 live births. Most often craniosynostosis occurs as an isolated (i.e. non‐syndromic) anomaly. Non‐syndromic craniosynostosis (NSC) is a clinically and genetically heterogeneous condition that has the characteristics of a multifactorial ...
Boyadjiev, Consortium, for the International Craniosynostosis   +1 more
openaire   +6 more sources

MYH3-associated non-syndromic palatoschisis (cleft palate, CP) in Limousine cattle. [PDF]

, 2023
We have successfully identified the most likely cause for a rare autosomal recessive disorder with only one case. Our clinicopathologic and genomic findings for the MYH3-related recessively inherited form of non-syndromic cleft palate are consistent with
Häfliger, Irene M, Eliana Schiavon, Coin, Patrizio, Jacinto, Joana G P, Schiavon, Eliana, Drögemüller, Cord, Patrizio Coin, Seefried, Franz R, Irene M. Häfliger, Cord Drögemüller, Joana G. P. Jacinto, Franz R. Seefried   +11 more
core   +1 more source

Academic achievement in non-syndromic craniosynostosis [PDF]

, 2023
A registry study on acadmic achievement in individuals with non-syndromic craniosynostosis (NSC)
Fotios C Papadopoulos, Karl Olsson, Mia Ramklint, Matilda A. Frick, Daniel Nowinski, Richard A White   +5 more
core   +1 more source

Syndromic and non-syndromic etiologies causing neonatal hypocalcemic seizures

Frontiers in Endocrinology, 2022
BackgroundThe diagnosis of neonatal hypocalcemic seizures (HS) in newborns is made based on clinical signs and serum calcium level. Their etiology is broad and diverse, and timely detection and initiation of treatment is essential.MethodsWe ...
Yi-Chieh Huang, Yin-Chi Chao, Inn-Chi Lee, Inn-Chi Lee   +3 more
doaj   +1 more source

Non syndromic unilateral posterior lenticonus

PAMJ Clinical Medicine, 2020
An 18 year-old girl presented with complaints of difficult in seeing distant objects with her left eye since childhood. On ocular examination: uncorrected visual acuity was determined by counting fingers 4 m for left eye, and 10/10 for the right eye. And
Narjisse Taouri, Imane Ed-Darraz
doaj   +1 more source

, a candidate gene for non‐syndromic rod‐cone dystrophy [PDF]

, 2021
Rod-cone dystrophy (RCD), also called retinitis pigmentosa, is characterized by rod followed by cone photoreceptor degeneration, leading to gradual visual loss.
Emmenegger, L, Leveillard, T, Marion Neuillé, Michiels, Christelle, Demontant, Vanessa, Vanessa Demontant, Christina Zeitz, Pierce, EA, Zeitz, C, Mohand-Saïd, Saddek, Zeitz, Christina, José‐Alain Sahel, Sahel, José-Alain, Eric A. Pierce, Emmenegger, Lisa, Lancelot, M-E, Neuillé, Marion, Neuille, M, Sahel, J-A, Bhattacharya, Shom Shanker, Marie‐Elise Lancelot, Maria Solaguren‐Beascoa, Condroyer, C, Wassila Carpentier, Letexier, M, Kinga M. Bujakowska, Saddek Mohand‐Saïd, Carpentier, Wassila, Carpentier, W, Solaguren-Beascoa, María, Elise Orhan, Orhan, Elise, Solaguren-Beascoa, M, Saraiva, J-P, Shomi S. Bhattacharya, Lancelot, Marie-Elise, Mohand-Said, S, Michiels, C, Audo, I, Christine Lonjou, Bhattacharya, SS, Christelle Michiels, Condroyer, Christel, Bujakowska, Kinga, Mejecase, C, Antonio, Aline, Lisa Emmenegger, Jean‐Paul Saraiva, Hélène Dollfus, Christel Condroyer, Méjécase, Cécile, Antonio, A, Aline Antonio, Orhan, E, Demontant, V, Isabelle Audo, Letexier, Mélanie, Lonjou, Christine, Bujakowska, KM, Mélanie Letexier, Audo, Isabelle, Cécile Méjécase, Dollfus, H, Saraiva, Jean-Paul, Dollfus, Hélène, Thierry Léveillard, Léveillard, Thierry, Lonjou, C, Pierce, Eric A.   +68 more
core   +1 more source