Výsledky vyhledávání - "L A, Bastiaensen"

On the cause of insidiously progressive diabetic blepharoptosis

Autor: L. A.K. Bastiaensen

Publikováno v: Neuro-Ophthalmology. 12:297-301

In many diabetics a slowly progressive blepharoptosis develops with intact upper eyelid crease, without signs of an n-III palsy. In 51 patients with diabetes I or II the height of the eyelid fissure was measured before and after topical application o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b4e3813cdd3e02c718b5b1a7fa5bb8eb
https://doi.org/10.3109/01658109209036985

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Ophthalmoplegia-plus

Autor: L A, Bastiaensen, H H, Jaspar, A M, Stadhouders

Publikováno v: Documenta Ophthalmologica. 46:365-380

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a04dd425749b94b6b71d514d0e179b11
https://doi.org/10.1007/bf00142628

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Conjunctival sarcoidosis

Autor: L A, Bastiaensen, M C, Verpalen, P M, Pijpers, A C, Sprong

Publikováno v: Documenta Ophthalmologica. 59:5-9

A biopsy from the lower conjunctival fornix, whether or not taken from follicles, is a method which yields a positive result in +/- 25% of cases of suspected sarcoidosis. We saw a patient with chronic recurrent follicular conjunctivitis of the upper

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::081371d8a047f4367395c39791682a60
https://doi.org/10.1007/bf00162003

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Oculopharyngodistal myopathy with early onset and neurogenic features

Autor: H H, Jaspar, L A, Bastiaensen, H J, ter Laak, E M, Joosten, M W, Horstink, A M, Stadhouders

Publikováno v: Clinical neurology and neurosurgery. 80(4)

Some clinical variants of oculopharyngeal dystrophy are known; a rare form is described in this article: the early-adult form of oculopharyngodistal myopathy. The diagnosis was made in 2 patients ((brother and sister) on the grounds of extensive clin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::61c21e8605c0ceb20d444f657e243021
https://pubmed.ncbi.nlm.nih.gov/216518

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Kearns syndrome or Kearns disease. Further evidence of a genuine entity in a case with uncommon features

Autor: L A, Bastiaensen, S L, Notermans, C H, Ramaekers, B J, van Dijke, E M, Joosten, H H, Jaspar, A M, Stadhouders, C T, Beljaars

Publikováno v: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde. 184(1)

A 20-year-old man with the characteristic findings of infantile onset Kearns syndrome is described. Morphological and biochemical investigations proved a mitochondrial disease which we believe to be the cause of the symptoms in various organs. We ass

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2bd10cb9855858d267e86a6ddc6b146d
https://pubmed.ncbi.nlm.nih.gov/7054739

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