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1. Full Text Amniotic band syndrome with placenta-encephalocele adhesion: An uncommon case
by da Silva, Aldo
Journal of pediatric neurosciences, ISSN 1817-1745, 4/2020, Volume 15, Issue 2, pp. 160 - 161
Encephalocele
Journal Article
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2. Full Text EP24.10: Diagnosis of encephalocele in a monochorionic diamniotic twin pregnancy in the first trimester and its management
by Eslamian, L and Marsoosi, V and Rahimian, H
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2019, Volume 54, Issue S1, pp. 394 - 394
Pregnancy | Encephalocele
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3. Full Text EP08.13: Appearance of the fetal posterior fossa at 11–14 weeks in fetuses with cephalocele
by Fanelli, T and Volpe, N and Campobasso, G and Salsi, G and Tempesta, A and Dall'Asta, A and Ghi, T and Volpe, P and Pilu, G
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 10/2018, Volume 52, Issue S1, pp. 225 - 225
Encephalocele | Fetuses
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4. Full Text Nasal encephaloceles: a review of etiology, pathophysiology, clinical presentations, diagnosis, treatment, and complications
by Tirumandas, Madhuri and Tirumandas, Madhuri and Sharma, Amit and Sharma, Amit and Gbenimacho, Ikechi and Gbenimacho, Ikechi and Shoja, Mohammadali M and Shoja, Mohammadali M and Tubbs, R Shane and Tubbs, R Shane and Oakes, W Jerry and Oakes, W Jerry and Loukas, Marios and Loukas, Marios
Child's nervous system, ISSN 0256-7040, 5/2013, Volume 29, Issue 5, pp. 739 - 744
Neurosciences | Medicine & Public Health | Nasal encephalocele | Neurosurgery | Basal encephalocele | Review | Frontoethmoidal encephalocele | Pediatrics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Surgery | Science & Technology | Encephalocele - diagnosis | Nose Diseases - etiology | Nose Diseases - surgery | Encephalocele - epidemiology | Humans | Encephalocele - classification | Nose Diseases - diagnosis | Encephalocele - etiology | Nose Diseases - epidemiology | Index Medicus
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5. Full Text EP02.09: Occipital cephalocele: diagnosis, obstetric and postnatal management
by Radulescu‐Botica, R and Toma, A and Diaconu, C and Alexandrescu, C
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 09/2017, Volume 50, Issue S1, pp. 263 - 263
Encephalocele | Diagnosis
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6. Full Text EP02.11: Posterior encephalocele with cerebellar displacement and hypolasia
by Kesrouani, A.K
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 09/2017, Volume 50, Issue S1, pp. 263 - 263
Encephalocele | Cerebellum
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7. Full Text Temporal bone encephalocele and cerebrospinal fluid fistula repair utilizing the middle cranial fossa or combined mastoid-middle cranial fossa approach
by Carlson, Matthew L and Copeland III, William R and Driscoll, Colin L and Link, Michael J and Haynes, David S and Thompson, Reid C and Weaver, Kyle D and Wanna, George B
Journal of neurosurgery, ISSN 0022-3085, 11/2013, Volume 119, Issue 5, pp. 1314 - 1322
Encephalocele | Cerebrospinal fluid leak | Temporal bone | Cerebrospinal fluid fistula | Idiopathic intracranial hypertension | Meningoencephalocele | Meningitis | Middle cranial fossa | Age Factors | Encephalocele - epidemiology | Humans | Middle Aged | Male | Young Adult | Adult | Female | Retrospective Studies | Fistula - complications | Child | Cranial Fossa, Middle - surgery | Fistula - cerebrospinal fluid | Neurosurgical Procedures - adverse effects | Mastoid - surgery | Fistula - epidemiology | Treatment Outcome | Encephalocele - etiology | Encephalocele - surgery | Encephalocele - complications | Temporal Bone - pathology | Temporal Bone - surgery | Adolescent | Sex Factors | Craniotomy - methods | Aged | Neurosurgical Procedures - methods | Fistula - etiology | Fistula - surgery | Index Medicus | Abridged Index Medicus
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8. Full Text Congenital nasal neuroglial heterotopia and encephaloceles: An update on current evaluation and management
by Adil, Eelam and Robson, Caroline and Perez‐Atayde, Antonio and Heffernan, Colleen and Moritz, Ethan and Goumnerova, Liliana and Rahbar, Reza
The Laryngoscope, ISSN 0023-852X, 09/2016, Volume 126, Issue 9, pp. 2161 - 2167
neuroglial heterotopia | encephalocele | Nasal glioma | congenital nasal lesion | Neuroglial heterotopia | Congenital nasal lesion | Encephalocele | Otorhinolaryngology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Encephalocele - diagnosis | Humans | Neuroglia | Nose Diseases - congenital | Child, Preschool | Infant | Male | Encephalocele - surgery | Nose Diseases - complications | Choristoma - diagnosis | Encephalocele - complications | Encephalocele - congenital | Nose Diseases - surgery | Nose Diseases - diagnosis | Choristoma - complications | Female | Retrospective Studies | Child | Choristoma - congenital | Choristoma - surgery | Infant, Newborn | Children's hospitals | Genetic disorders | Diagnosis | Plastic surgery | Breasts | Endoscopy | Index Medicus
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9. Full Text Meckel-Gruber Syndrome: A population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe
by Barisic, Ingeborg and Boban, Ljubica and Loane, Maria and Garne, Ester and Wellesley, Diana and Calzolari, Elisa and Dolk, Helen and Addor, Marie-Claude and Bergman, Jorieke E. H and Braz, Paula and per, Elizabeth S and Haeusler, Martin and Khoshnood, Babak and Klungsoyr, Kari and Pierini, Anna and Queisser-Luft, Annette and Rankin, Judith and Rissmann, Anke and Verellen-Dumoulin, Christine
European journal of human genetics : EJHG, ISSN 1018-4813, 06/2015, Volume 23, Issue 6, pp. 746 - 752
CRITERIA | SHH | ANOMALIES | NEURAL-TUBE DEFECTS | PHENOTYPES | MUTATIONS | SPECTRUM | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Ciliary Motility Disorders - epidemiology | Polycystic Kidney Diseases - genetics | Prenatal Diagnosis - statistics & numerical data | Encephalocele - diagnosis | Polycystic Kidney Diseases - diagnosis | Prevalence | Encephalocele - epidemiology | Genetic Testing - statistics & numerical data | Europe | Humans | Polycystic Kidney Diseases - mortality | Male | Encephalocele - mortality | Pregnancy | Ciliary Motility Disorders - mortality | Ciliary Motility Disorders - diagnosis | Female | Polycystic Kidney Diseases - epidemiology | Ciliary Motility Disorders - genetics | Encephalocele - genetics | Dysplasia | Kidneys | Congenital defects | Fetuses | Liver | Central nervous system | Nervous system | Population studies | Neurodevelopmental disorders | Orofacial clefts | Epidemiology | Genetic screening | Encephalocele | Ultrasonic imaging | Hospitals | Prenatal diagnosis | Polydactyly | Population | Genetics | Mutation | Public health | Index Medicus
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10. Full Text Encephalocele With Areas Mimicking Giant Cell Fibroblastoma
by Li, Rong and Ma, Yihong and Rozelle, Curtis and Kelly, David
American journal of clinical pathology, ISSN 0002-9173, 10/2014, Volume 142, Issue suppl_1, pp. A005 - A005
Encephalocele | Mimicry
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11. Full Text OC16.04: Intrauterine open fetal surgery for correction of isolated occipital encephalocele
by Milani, H.J and Barbosa, M.M and Sarmento, S and Cavalheiro, S and Suriano, I and Moron, A.F
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 09/2017, Volume 50, Issue S1, pp. 33 - 34
Encephalocele | Surgery | Fetuses
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12. Full Text MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis
by Williams, Corey L and Li, Chunmei and Kida, Katarzyna and Inglis, Peter N and Mohan, Swetha and Semenec, Lucie and Bialas, Nathan J and Stupay, Rachel M and Chen, Nansheng and Blacque, Oliver E and Yoder, Bradley K and Leroux, Michel R
The Journal of cell biology, ISSN 0021-9525, 03/2011, Volume 192, Issue 6, pp. 1023 - 1041
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Cilia - physiology | Polycystic Kidney Diseases - genetics | Ciliary Motility Disorders - physiopathology | Humans | Caenorhabditis elegans Proteins - metabolism | Recombinant Fusion Proteins - metabolism | Caenorhabditis elegans - physiology | Polycystic Kidney Diseases - pathology | Polycystic Kidney Diseases - physiopathology | Protein Isoforms - metabolism | Cilia - ultrastructure | Kidney Diseases, Cystic - genetics | Membrane Proteins - metabolism | Encephalocele - genetics | Kidney Diseases, Cystic - physiopathology | Membrane Proteins - genetics | Rats | Encephalocele - physiopathology | Kidney Diseases, Cystic - pathology | Animals | Ciliary Motility Disorders - pathology | Encephalocele - pathology | Recombinant Fusion Proteins - genetics | Caenorhabditis elegans Proteins - genetics | Kidney Diseases, Cystic - congenital | Ciliary Motility Disorders - genetics | Protein Isoforms - genetics | Causes of | Cell physiology | Research | Meckel-Gruber syndrome | Health aspects | Cell cycle | Proteins | Nematodes | Genotype & phenotype | Membranes | Genetic disorders | Cellular biology | Index Medicus
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13. Frontoethmoidal encephalocele. Report of a case
by Horcajadas, Angel and Palma, Antonio and Khalon, Babar M
Neurocirugía (Asturias, Spain), ISSN 1130-1473, 03/2019, Volume 30, Issue 2, pp. 94 - 99
Encephalocele | Nasal encephalocele | Congenital malformation | Frontoethmoidal encephalocele | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Surgery | Science & Technology | Female | Encephalocele - diagnosis | Encephalocele - surgery | Ethmoid Bone | Humans | Infant, Newborn
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14. Full Text Epilepsy with temporal encephalocele: Characteristics of electrocorticography and surgical outcome
by Panov, Fedor and Li, Yi and Chang, Edward F and Knowlton, Robert and Cornes, Susannah B
Epilepsia (Copenhagen), ISSN 0013-9580, 02/2016, Volume 57, Issue 2, pp. e33 - e38
Encephalocele | Temporal epilepsy | Meningoencephalocele | Surgical outcome | Electrocorticography | Drug Resistant Epilepsy - diagnosis | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Electroencephalography | Epilepsy, Temporal Lobe - surgery | Temporal Lobe - diagnostic imaging | Temporal Lobe - surgery | Young Adult | Epilepsy, Temporal Lobe - diagnosis | Drug Resistant Epilepsy - etiology | Adult | Female | Retrospective Studies | Temporal Lobe - pathology | Encephalocele - diagnosis | Anterior Temporal Lobectomy | Treatment Outcome | Epilepsy, Temporal Lobe - etiology | Encephalocele - surgery | Encephalocele - complications | Magnetic Resonance Imaging | Temporal Lobe - physiopathology | Drug Resistant Epilepsy - surgery | Cohort Studies | Epilepsy | Surgical outcomes | Medical imaging | Index Medicus
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15. Full Text Prenatal diagnosis of familial atretic encephalocele
by Lau, W. L and Yung, W. Y and Leung, W. C and Kan, A and Chan, K and Luk, H. M and Kan, E and Lam, Y. Y
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 08/2019, Volume 54, Issue 2, pp. 277 - 279
Acoustics | Life Sciences & Biomedicine | Technology | Radiology, Nuclear Medicine & Medical Imaging | Obstetrics & Gynecology | Science & Technology | Occipital Bone - abnormalities | Humans | Magnetic Resonance Imaging - methods | Treatment Outcome | Fetal Diseases - diagnostic imaging | Encephalocele - surgery | Homeodomain Proteins - genetics | Occipital Bone - diagnostic imaging | Fetal Diseases - genetics | Pregnancy | Young Adult | Encephalocele - congenital | Amniocentesis - methods | Cytogenetics - methods | Female | Encephalocele - diagnostic imaging | Prenatal Diagnosis - methods | Karyotype | Encephalocele | Genetic aspects | Diagnostic imaging | Pregnant women | Prenatal diagnosis
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16. Diagnosis of endocrine disease: Primary empty sella: A comprehensive review
by Chiloiro, S and Giampietro, A and Bianchi, A and Tartaglione, T and Capobianco, A and Anile, C and De Marinis, L
European journal of endocrinology, ISSN 0804-4643, 12/2017, Volume 177, Issue 6, pp. R275 - R285
Neuroimaging | Pituitary Gland - metabolism | Subarachnoid Space - physiopathology | Humans | Subarachnoid Space - diagnostic imaging | Human Growth Hormone - deficiency | Sella Turcica - diagnostic imaging | Asymptomatic Diseases | Intracranial Hypertension - prevention & control | Human Growth Hormone - metabolism | Pituitary Gland - physiopathology | Hyperprolactinemia - prevention & control | Intracranial Hypertension - etiology | Sella Turcica - physiopathology | Severity of Illness Index | Encephalocele - diagnosis | Encephalocele - therapy | Pituitary Gland - diagnostic imaging | Encephalocele - physiopathology | Magnetic Resonance Imaging | Empty Sella Syndrome - diagnosis | Empty Sella Syndrome - therapy | Papilledema - prevention & control | Empty Sella Syndrome - physiopathology | Encephalocele - diagnostic imaging | Hyperprolactinemia - etiology | Empty Sella Syndrome - diagnostic imaging | Papilledema - etiology | Hypertension | Subarachnoid space | Headache | Optic nerve | Swelling | Hyperprolactinemia | Body weight | Cerebrospinal fluid | Acuity | Pituitary | Nose | Diaphragm | Diagnosis | Growth hormone
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17. Full Text Procalcitonin as a biomarker for malignant cerebral edema in massive cerebral infarction
by Zhang, Yan and Liu, Gang and Wang, Yuan and Su, Yingying and Leak, Rehana K and Cao, Guodong
Scientific reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 993 - 6
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prospective Studies | Area Under Curve | Humans | Middle Aged | Brain Neoplasms - pathology | Cerebral Infarction - diagnosis | Male | Encephalocele - mortality | Phosphopyruvate Hydratase - blood | Cerebral Infarction - blood | Brain Neoplasms - blood | Brain Edema - diagnosis | Brain Edema - mortality | Female | Leukocyte Count | Brain Neoplasms - mortality | Odds Ratio | Cerebral Infarction - pathology | Neutrophils - pathology | Calcitonin - blood | Encephalocele - diagnosis | Encephalocele - blood | Brain Edema - pathology | Brain Neoplasms - diagnosis | Cerebral Infarction - mortality | Logistic Models | Body Temperature | Biomarkers, Tumor - blood | Encephalocele - pathology | Survival Analysis | Aged | Brain Edema - blood | Edema | Cerebral infarction | Body temperature | Procalcitonin | Neutrophils | Death | Drug overdose | Risk factors | Phosphopyruvate hydratase | Index Medicus
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18. Full Text Collagen XVIII in tissue homeostasis and dysregulation — Lessons learned from model organisms and human patients
by Heljasvaara, Ritva and Aikio, Mari and Ruotsalainen, Heli and Pihlajaniemi, Taina
Matrix biology, ISSN 0945-053X, 01/2017, Volume 57-58, Issue 1, pp. 55 - 75
Knobloch syndrome | Multiplexin | Heparan sulphate proteoglycan | Basement membrane | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Neoplasms - metabolism | Endostatins - pharmacology | Retinal Detachment - pathology | Basement Membrane - drug effects | Humans | Basement Membrane - pathology | Encephalocele - metabolism | Neovascularization, Pathologic - pathology | Protein Isoforms - metabolism | Neoplasms - genetics | Proteolysis | Protein Domains | Neovascularization, Pathologic - prevention & control | Encephalocele - genetics | Retinal Detachment - metabolism | Gene Expression Regulation | Retinal Detachment - congenital | Recombinant Proteins - pharmacology | Retinal Detachment - genetics | Basement Membrane - metabolism | Cell Movement - drug effects | Animals | Encephalocele - pathology | Collagen Type VIII - metabolism | Neovascularization, Pathologic - genetics | Cell Proliferation - drug effects | Neovascularization, Pathologic - metabolism | Neoplasms - pathology | Homeostasis - genetics | Collagen Type VIII - genetics | Endothelial Cells - drug effects | Protein Isoforms - genetics | Collagen | Analysis | Mice | Peptides | Cell differentiation | Stem cells | Cell culture | Membranes | Animal models | Genetic disorders | Cell survival | Wnt protein | Frizzled protein | Endostatin | Homeostasis | C-Terminus | Progenitor cells | Endothelial cells | Angiogenesis | Encephalocele | Laminin | Isoforms | Mutation | Collagen (type XVIII) | Cell migration | Thrombospondin | Tumors | Index Medicus
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