Results 241 to 250 of about 22,934 (282)
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Palato-Pharyngo-Laryngeal Rhythmic Myoclonus in Neuro-Behcet Syndrome: A Case Report
Annals of Otology, Rhinology and Laryngology, 2022Objective: Behcet’s syndrome (BS) is a chronic, relapsing multisystemic inflammatory perivasculitis and can affect any tissue, including the nervous system.
D. Kothari +4 more
semanticscholar +1 more source
Journal of Esthetic and Restorative Dentistry, 2021
OBJECTIVE The palato-radicular groove (PRG) is caused by a developmental anomaly, genetically determined, whereby an in-folding of the enamel organ and Hertwig's epithelial root sheath occurs.
D. Mathews, David E. Hansen
semanticscholar +1 more source
OBJECTIVE The palato-radicular groove (PRG) is caused by a developmental anomaly, genetically determined, whereby an in-folding of the enamel organ and Hertwig's epithelial root sheath occurs.
D. Mathews, David E. Hansen
semanticscholar +1 more source
The Indian Journal of Pediatrics, 1970
A female child showed features of deafness, characteristic facies and a generalized bone dysplasia, and was diagnosed to have the “oto-palatal-digital syndrome”. The literature is briefly reviewed.
S. D. Singh, M. Irani, M. S. Diwedi
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A female child showed features of deafness, characteristic facies and a generalized bone dysplasia, and was diagnosed to have the “oto-palatal-digital syndrome”. The literature is briefly reviewed.
S. D. Singh, M. Irani, M. S. Diwedi
openaire +3 more sources
The oto-palato-digital syndrome
The Journal of Laryngology & Otology, 1976A boy aged ten years with oto-palato-digital syndrome is discussed. Because of severe conductive hearing loss tympanotomy was performed and abnormal poorly mobile ossicles were found. Stapedectomy was performed without improvement of hearing.
M. Fradis, L. Podoshin, H. S. A. Heymans
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Lipossarcoma bem diferenciado de palato mole: relato de caso e revisão da literatura
, 2021O lipossarcoma é um tumor maligno mesenquimal originado a partir de células do tecido adiposo. Incide, predominantemente, nas extremidades e retroperitônio, sendo raro na região da cabeça e pescoço, em especial na orofaringe.
Júlio Cláudio Sousa +3 more
semanticscholar +1 more source
INHERITANCE OF THE OTO-PALATO-DIGITAL SYNDROME
Archives of Pediatrics & Adolescent Medicine, 1970To the Editor .—Dudding et al 1 in 1967 reported a family with multiple defects and suggested it be called the oto-palato-digital syndrome. In the sibship described there were three affected male subjects. It was suggested that the entity was probably autosomal recessive but could be X-linked.
G, Turner, R J, Gorlin
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Clinical strategies for successful palato-mesiobuccal canal management-Report of 2 cases.
International Endodontic JournalAIM To describe the management of the palato-mesiobuccal (PMB) canal in maxillary second molars with fused roots using conventional techniques. SUMMARY Root canal treatment success hinges upon effectively addressing the intricate and variable anatomy ...
D. Kudryashov, M. Versiani
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#010 Lesão violácea do palato: Um desafio Diagnóstico
Revista Portuguesa de Estomatologia, Medicina Dentaria e Cirurgia MaxilofacialIntrodução: O mucocelo é uma lesão benigna resultante da alteração do fluxo salivar das glândulas salivares minor em contexto de trauma ou obstrução (inflamação crónica, fibrose ductal, sialolitíase, neoplasia).
C. Barros +5 more
semanticscholar +1 more source
The Oto-palato-digital (OPD) Syndrome
Archives of Otolaryngology - Head and Neck Surgery, 1967TAYBI described a case of "generalized skeletal dysplasia with multiple anomalies" in 1962 which did not fit any previously described disease complex. 1 This paper will present three male siblings seen at the University of Minnesota Hospitals with the same spectrum of anomalies.
David J. Buran, Arndt J. Duvall
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Archives of Pediatrics & Adolescent Medicine, 1967
To the Editor .—With regard to our paper (Amer J Dis Child113:214-221, 1967), entitled "Oto-Palato-Digital Syndrome" we have seen another case in a boy who also had identical facies and in the Journal of Medical Genetics 3:17-22, 1966, there appeared to be four other cases reported in boys. This would clearly indicate that this syndrome is inherited as
openaire +3 more sources
To the Editor .—With regard to our paper (Amer J Dis Child113:214-221, 1967), entitled "Oto-Palato-Digital Syndrome" we have seen another case in a boy who also had identical facies and in the Journal of Medical Genetics 3:17-22, 1966, there appeared to be four other cases reported in boys. This would clearly indicate that this syndrome is inherited as
openaire +3 more sources