Results 151 to 160 of about 1,323 (194)
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Anterior Fontanel Meningoencephalocele
Radiology, 1972The authors report an extraordinary meningoencephalocele, 20 em in diameter, presenting through the anterior fontanel in a neonate. Craniolacunae were noted on plain skull films and severe parenchymal abnormalities were demonstrated by cerebral angiography and pneumoencephalagraphy, Surgical excision of the meningoencephalocele permitted the infant to ...
William L Schey
exaly +3 more sources
Hypopituitarism associated with transsphenoidal meningoencephalocele
European Journal of Pediatrics, 1982A 12-year-old boy with growth hormone deficiency and partial diabetes insipidus resulting from transsphenoidal meningoencephalocele and with eye abnormalities is described. Fifteen other patients with transsphenoidal meningoencepalocele have been reported. Hypothalamic-pituitary dysfunctions were diagnosed by endocrinological studies in seven cases. It
Takeshi Usui, K Sakoda
exaly +3 more sources
Intradiploic meningoencephalocele
European Radiology, 2002We report on a 36-year-old patient who presented with coordinative problems in his right leg. The MRI study of his brain showed the extremely rare intradiploic meningoencephalocele which explained his symptoms. Most cephaloceles are inborn developmental disturbances and present with symptoms of different severity depending on the degree of associated ...
Jutta, Peters +3 more
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Anterior orbital meningoencephalocele
European Archives of Oto-Rhino-Laryngology, 2010Basal and syncipital meningoceles and meningoencephaloceles are relatively rare. Otorhinolaryngologists, neurologists, and ophthalmologists should know all the details concerning their incidence, diagnosis, and differential diagnosis. Incorrect interpretation of formations propagating especially into the nasal cavity or the paranasal sinuses and ...
Arnost, Pellant +2 more
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Meningoencephalocele of the paranasal sinuses
The Laryngoscope, 1975AbstractMeningoencephaloceles are not commonly seen by the otolaryngologist. They occur most frequently in the lumbosacral area where they are five times as common as in the occipital area. The anterior cranial presentation is quite rare.Most patients with meningoencephaloceles present early with large lesions and are treated by the neurosurgeon.
A M, Kane, J, Loré
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Hereditary meningoencephalocele in Burmese cats
Journal of Heredity, 1986A syndrome of meningoencephalocele and related craniofacial abnormalities occurred in 19 (6 male, 3 female, 10 of unknown sex) of 88 kittens in 22 litters born to matings between Burmese cats that were known to produce this defect. This is consistent with the action of an autosomal recessive gene.
D P, Sponenberg, E, Graf-Webster
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Surgical Treatment of a Meningoencephalocele in a Cat
Veterinary Surgery, 2011Objective: To report the clinical signs, imaging findings and surgical treatment of a meningoencephalocele in a cat.Study Design: Case report.Animal: Domestic shorthaired cat, 4 months old.Methods: A parietal meningoencephalocele was identified and characterized by magnetic resonance and computed tomography (CT) imaging.
Curtis W, Dewey +4 more
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Infratorcular Meningoencephalocele with Dermoid Cyst
Pediatric Neurosurgery, 2010Encephalocele represents one end of the spectrum of open neural tube defects. We report an infant with Chiari type 3 malformation manifesting as infratorcular occipital meningoencephalocele with dermoid cyst. To our knowledge, this is the first time that this association is described.
Amit, Mahore +5 more
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The Frontal Sinus in Frontoethmoidal Meningoencephaloceles
Journal of Craniofacial Surgery, 1994We performed a review of all patients with frontoethmoidal meningoencephaloceles (FEME) in whom frontal sinus development would be expected to be complete. Frontal sinus absence is the predominant finding. The potential role of the FEME in producing a structural blockage to normal frontal sinus development is suggested.
M H, Moore, S, Blackwell, M, Butterworth
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Intranasal Meningoencephalocele
Archives of Otolaryngology - Head and Neck Surgery, 1974P H, Schmidt, W, Leyendiijk
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