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microphthalmos/glavobolja

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ČlanciKliničkim ispitivanjimaPatenti
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Nanophthalmos patient with a THR518MET mutation in MYRF, a case report

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Background: Nanophthalmos has a significant genetic background and disease-causing mutations have been recently been reported in the myelin regulatory factor (MYRF) gene. We report clinical features in a patient with nanophthalmos and a

Tuberous sclerosis associated with histologically confirmed ocular and cerebral tumors.

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The clinical, neuroradiologic, and pathologic features of an unusual retinal and cerebral giant cell astrocytoma in a 24-year-old man with tuberous sclerosis are reported. The patient was referred at 3 years of age because of partial seizures from the first months of life, severe mental retardation,

Intracranial arachnoid cysts in children: related signs and associated anomalies.

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Intracranial arachnoid cysts are benign development anomalies that may be clinically asymptomatic. The authors describe 30 children with intracranial arachnoid cysts in terms of clinical manifestations and relations to the associated brain anomalies or lesions. The mean age at onset of clinical
Fargesin is commonly used in the treatment of allergic rhinitis, inflammation, sinusitis and headache.The aim of the study is to investigate a new function of fargesin against melanin production and its underlying molecular

Antimelanoma activity of perphenazine and prochlorperazine in human COLO829 and C32 cell lines.

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Cutaneous melanoma is least common (only about 1% of skin cancers) but is the deadliest malignant tumor. Moreover, amelanotic types of melanoma are very difficult for clinical diagnosis. The standard therapy can cause a lot of side effects, e.g., nausea, vomiting, and headaches, which means that
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