Results 171 to 180 of about 21,962 (215)
Some of the next articles are maybe not open access.
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 S, Diwedi, M, Irani
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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 S, Diwedi, M, Irani
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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
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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
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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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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.
D J, Buran, A J, Duvall
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Palato-ocular Synchrony During Eyelid Closure
Archives of Neurology, 1976The effects of eyelid closure on oculomotor function was examined in 11 patients with palatal myoclonus. In eight patients, eyelid closure induced gross rhythmic vertical or almost oscillatory movements of the globes, which were synchronous with the rhythmic beat of the palatal myoclonus. The rhythmic vertical ocular movements induced by eyelid closure
L, Jacobs, M B, Bender
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Macroscopic and Microscopic Analysis of the Palato-Gingival Groove
Journal of Endodontics, 2000With the objective of correlating the anatomical aspects of the palato-gingival groove with its etiology, diagnosis, and alternative treatments, 13 permanent maxillary incisors with palato-gingival grooves were selected from a large sample and subjected to macroscopic and microscopic analysis of groove morphology.
V S, Lara, A, Consolaro, R S, Bruce
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2007
Per molti dei giallisti «mediterranei» il palato dei loro eroi è di fondamentale importanza. Nasce così tutta una schiera di investigatori gourmet che alla scena del giallo aggiungono il sapore, come antidoto o consolazione al delitto.
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Per molti dei giallisti «mediterranei» il palato dei loro eroi è di fondamentale importanza. Nasce così tutta una schiera di investigatori gourmet che alla scena del giallo aggiungono il sapore, come antidoto o consolazione al delitto.
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[Palato-pharyngo-laryngeal myoclonus].
Nihon rinsho. Japanese journal of clinical medicine, 1994Palato-pharyngo-laryngeal myoclonus is well-known clinical criterion characterized by persistent, rapid, repetitive, rhythmic muscle twitch the rate of which ranges 50-200 Hz. It appears in the palate, pharynx, larynx, diaphragma, and the ocular or limb muscles, but the most common combination of the distribution is palate-pharyngo-laryngeal type or ...
M, Kinoshita, E, Satoyoshi, Y, Araki
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A Case of ‘Palato-Pharyngeal Myoclonus’
Gerontologia Clinica, 1969D B, Rao, M S, Kataria
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