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by Xu, WR and Zhao, JL and Zhu, YC and Zhang, WH
MEDICINE, ISSN 0025-7974, 01/2017, Volume 96, Issue 1, p. e5545
Rational: Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) is believed to be an autosomal recessive genetic disease, with disorders in... 
inherited diseases | CTC1 | cerebral calcification | cerebroretinal microangiopathy with calcifications and cysts | COMPONENT 1 | MEDICINE, GENERAL & INTERNAL | DISEASE | leukoencephalopathy | DISORDER | case report | MUTATIONS | Calcinosis - genetics | Aftercare - methods | Retinal Diseases - genetics | Brain - diagnostic imaging | Calcinosis - diagnosis | Leukoencephalopathies - genetics | Central Nervous System Cysts - physiopathology | Seizures - genetics | Humans | Brain Neoplasms - physiopathology | Retinal Diseases - therapy | Leukoencephalopathies - physiopathology | Proton Magnetic Resonance Spectroscopy - methods | Muscle Spasticity - therapy | Seizures - physiopathology | Telomere-Binding Proteins - genetics | Leukoencephalopathies - diagnosis | Adult | Central Nervous System Cysts - diagnosis | Female | Ataxia - genetics | Central Nervous System Cysts - therapy | Neuroimaging - methods | Ataxia - physiopathology | Ataxia - therapy | Diagnosis, Differential | Retinal Diseases - diagnosis | Brain Neoplasms - diagnosis | Brain Neoplasms - genetics | Seizures - diagnosis | Seizures - therapy | Ataxia - diagnosis | Disease Progression | Central Nervous System Cysts - genetics | Calcinosis - therapy | Brain Neoplasms - therapy | Brain - pathology | Muscle Spasticity - diagnosis | Leukoencephalopathies - therapy | Disease Management | Muscle Spasticity - physiopathology | Mutation | Retinal Diseases - physiopathology | Muscle Spasticity - genetics | Calcinosis - physiopathology | Care and treatment | Usage | Vasculitis | Diagnosis | Cysts | Lasers in surgery
Journal Article
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 02/2012, Volume 76, Issue 2, pp. 151 - 160
Journal Article
World Neurosurgery, ISSN 1878-8750, 01/2020, Volume 133, pp. e241 - e251
Journal Article
World Neurosurgery, ISSN 1878-8750, 2017, Volume 104, pp. 509 - 515
Abstract Introduction Management of high grade glioma (HGG) was changed by recent landmark trials and is nowadays more proactive. However, aggressive treatment... 
Neurosurgery | Tumor bed cyst | High-grade glioma | Cerebrospinal fluid shunt | Glioblastoma | SURGERY | SURVIVAL | WAFER IMPLANTATION | RESECTION | HYDROCEPHALUS | CHEMOTHERAPY | CLINICAL NEUROLOGY | TRIAL | ADJUVANT RADIOCHEMOTHERAPY | MALIGNANT GLIOMAS | Cerebral Ventricles - surgery | Glioma - classification | Glioma - diagnosis | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Supratentorial Neoplasms - diagnosis | Chemoradiotherapy, Adjuvant | Supratentorial Neoplasms - classification | Young Adult | Glioma - pathology | Aged, 80 and over | Brain Edema - diagnosis | Adult | Central Nervous System Cysts - classification | Central Nervous System Cysts - diagnosis | Female | Glioblastoma - classification | Retrospective Studies | Brain Edema - classification | Glioma - surgery | Cerebral Ventricles - pathology | Glioblastoma - diagnosis | Supratentorial Neoplasms - pathology | Brain Edema - pathology | Central Nervous System Cysts - surgery | Combined Modality Therapy | Cranial Irradiation | Neoplasm Grading - classification | Supratentorial Neoplasms - surgery | Central Nervous System Cysts - pathology | Glioblastoma - surgery | Magnetic Resonance Imaging | Brain Edema - surgery | Glioblastoma - pathology | Adolescent | Craniotomy | Aged | Carmustine - administration & dosage | Care and treatment | Cysts | Gliomas | Analysis
Journal Article
Journal of Neurology, ISSN 0340-5354, 10/2014, Volume 261, Issue 10, pp. 1911 - 1916
We present a clinical, neuro-radiological and genetic study on a family with members suffering from an autosomal dominantly inherited syndrome characterised by... 
Neurology | Neurosciences | Coats plus disease | Cerebral calcifications | Medicine & Public Health | CRMCC | Labrune syndrome | LCC | Neuroradiology | COMPLEX | TINF2 | CEREBRORETINAL MICROANGIOPATHY | CLINICAL NEUROLOGY | RETINOPATHY | COMPONENT | MUTATIONS | APLASTIC-ANEMIA | Calcinosis - genetics | Retinal Diseases - genetics | Calcinosis - diagnosis | Leukoencephalopathies - genetics | Calcinosis - complications | Seizures - genetics | Humans | Family Health | Male | Tomography, X-Ray Computed | Brain Neoplasms - complications | Seizures - complications | Telomere-Binding Proteins - genetics | Leukoencephalopathies - diagnosis | Central Nervous System Cysts - diagnosis | Female | Ophthalmology | Ataxia - genetics | Retinal Diseases - diagnosis | Retinal Diseases - complications | Brain Neoplasms - diagnosis | Brain Neoplasms - genetics | Seizures - diagnosis | Mutation - genetics | Ataxia - diagnosis | Central Nervous System Cysts - genetics | Magnetic Resonance Imaging | Muscle Spasticity - complications | Leukoencephalopathies - complications | Muscle Spasticity - diagnosis | Central Nervous System Cysts - complications | Ataxia - complications | Muscle Spasticity - genetics | Complications and side effects | Care and treatment | Epilepsy | Development and progression | Research | Leukoencephalopathy | Health aspects
Journal Article
by Bian, BY and Yu, M and Liu, SS and Li, S and Wei, Y and Zhang, B
MEDICINE, ISSN 0025-7974, 07/2019, Volume 98, Issue 30, p. e16650
Rationale: Bronchogenic cysts are mainly benign, congenital abnormalities, originating from the remnants of the primitive foregut. However, intracranial... 
bronchogenic cysts | central nervous system cyst | MEDICINE, GENERAL & INTERNAL | diagnosis | suprasellar region | Case studies | Care and treatment | Diagnosis | Cysts | Brain diseases
Journal Article
Radiographics, ISSN 0271-5333, 03/2012, Volume 32, Issue 2, pp. 499 - 516
Various substances, including methemoglobin, melanin, lipid, protein, calcium, iron, copper, and manganese, are responsible for the intrinsically high signal... 
CEREBRAL AMYLOID ANGIOPATHY | IMAGING FINDINGS | ECTOPIC POSTERIOR | VENOUS THROMBOSIS | GLOBUS-PALLIDUS | BASAL GANGLIA LESIONS | RATHKE CLEFT CYSTS | SURGICAL-TREATMENT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | CORTICAL LAMINAR NECROSIS | NEUROFIBROMATOSIS TYPE-1 | Brain Diseases - metabolism | Humans | Middle Aged | Brain Neoplasms - pathology | Child, Preschool | Magnetic Resonance Imaging - methods | Infant | Male | Proteins - analysis | Genetic Diseases, Inborn - pathology | Cerebral Amyloid Angiopathy - metabolism | Sinus Thrombosis, Intracranial - diagnosis | Cysts - metabolism | Hemangioma, Cavernous, Central Nervous System - chemistry | Melanins - analysis | Brain Neoplasms - secondary | Adult | Female | Genetic Diseases, Inborn - metabolism | Child | Genetic Diseases, Inborn - diagnosis | Brain Neoplasms - chemistry | Diagnosis, Differential | Cerebral Amyloid Angiopathy - diagnosis | Brain Diseases - diagnosis | Brain Neoplasms - diagnosis | Minerals - analysis | Cysts - pathology | Cerebral Amyloid Angiopathy - pathology | Brain Diseases - pathology | Hemangioma, Cavernous, Central Nervous System - pathology | Brain - pathology | Brain Chemistry | Cysts - diagnosis | Hemangioma, Cavernous, Central Nervous System - diagnosis | Lipids - analysis | Pituitary Gland | Methemoglobin - analysis | Sinus Thrombosis, Intracranial - pathology
Journal Article
Journal Article