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Enzyme immobilization in biodegradable polymers for biomedical applications [PDF]
Azevedo, Helena S. +2 more
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Journal of the European Academy of Dermatology and Venereology, 2003
ABSTRACTOculocutaneous albinism represents a group of inherited skin disorders characterized by a generalized reduction of cutaneous, ocular and pilar pigmentation from the time of birth. Oculocutaneous albinism types 1 and 2 are the most common, but several other types have been described.
J F, Okulicz +3 more
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ABSTRACTOculocutaneous albinism represents a group of inherited skin disorders characterized by a generalized reduction of cutaneous, ocular and pilar pigmentation from the time of birth. Oculocutaneous albinism types 1 and 2 are the most common, but several other types have been described.
J F, Okulicz +3 more
openaire +2 more sources
Oculocutaneous albinism and schizophrenia
Biological Psychiatry, 1986rodents, albinos showed marked behavioral differences from their pigmented counterparts (Henry and Schlesinger 1967). Greiner and Nicolson (1965) proposed a relationship between hypermelanosis and schizophrenia, noting increased melanogenesis in autopsy material from schizophrenics institutionalized in the prephenothiazine era. They hypothesized that a
M H, Pollack, T C, Manschreck
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Newborn With Oculocutaneous Albinism
Journal of Pediatric Health Care, 2014MEDICAL AND OBSTETRICAL HISTORY Themother’s medical historywas benign except for excision of a gangrenous lesion from her right hand. Her obstetrical history was not significant for any previous genetic disorders. She was identified as gravida 4, para 1.
Ebony, Beaudoin +2 more
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RETINOBLASTOMA IN OCULOCUTANEOUS ALBINISM
RETINAL Cases & Brief Reports, 2010To report a case of retinoblastoma in a child with oculocutaneous albinism (OCA).A 24-month-old girl with classic features of OCA developed leukocoria in the left eye.The patient was found to have an endophytic retinoblastoma and an exophytic retinoblastoma, with a total retinal detachment and neovascularization of the iris. Enucle-ation was performed,
Fariba, Ghassemi +4 more
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Annales de pediatrie, 1992
Oculocutaneous albinism (OCA) is an inherited condition characterized by hypopigmentation of the skin, hair, and eyes. Ocular involvement is often severe with photophobia, decreased visual acuity due to foveal hypoplasia, nystagmus, and strabism secondary to defective routing of optic axons in the chiasma.
J P, Lacour, J P, Ortonne
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Oculocutaneous albinism (OCA) is an inherited condition characterized by hypopigmentation of the skin, hair, and eyes. Ocular involvement is often severe with photophobia, decreased visual acuity due to foveal hypoplasia, nystagmus, and strabism secondary to defective routing of optic axons in the chiasma.
J P, Lacour, J P, Ortonne
openaire +1 more source
Developmental glaucoma in oculocutaneous albinism
Ophthalmic Paediatrics and Genetics, 1988A case of oculocutaneous albinism is described in which bilateral Axenfeld's anomaly co-exists. Progressive elevation of intraocular pressure required treatment and this complication has not been reported. Different hypotheses regarding the co-existence of these conditions are reviewed.
D F, Larkin, H N, O'Donoghue
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