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1. 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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2. 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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3. 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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4. 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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5. Transsellar transsphenoidal encephalocele: A series of four cases
by Rathore, Yashpal S and Sinha, Sumit and Mahapatra, A.K
12/2011
Transsellar transsphenoidal encephalocele is the least common type of basal encephalocele. We present a series of four cases of transsellar transsphenoidal... 
transsellar transsphenoidal encephalocele | transpalatal approach | Basal encephalocele
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6. Full Text Nasal encephaloceles: a review of etiology, pathophysiology, clinical presentations, diagnosis, treatment, and complications
by Tirumandas, Madhuri and Sharma, Amit and Gbenimacho, Ikechi and Shoja, Mohammadali M and Tubbs, R Shane and Oakes, W Jerry and Loukas, Marios
Child's Nervous System, ISSN 0256-7040, 5/2013, Volume 29, Issue 5, pp. 739 - 744
Encephaloceles are considered by most to be a type of neural tube defect characterized by a herniation of the brain and meninges through structural weaknesses... 
Neurosciences | Medicine & Public Health | Nasal encephalocele | Neurosurgery | Basal encephalocele | Review | Frontoethmoidal encephalocele | SURGERY | FRONTOETHMOIDAL ENCEPHALOMENINGOCELE | SERIES | PERIOPERATIVE MANAGEMENT | PEDIATRICS | MENINGOENCEPHALOCELE | CLINICAL NEUROLOGY | CHILDREN | Encephalocele - diagnosis | Nose Diseases - etiology | Nose Diseases - surgery | Encephalocele - epidemiology | Humans | Encephalocele - classification | Nose Diseases - diagnosis | Encephalocele - etiology | Nose Diseases - epidemiology
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7. Spina bifida and cranium bifidum
: Papers reprinted from the New England journal of medicine, with the addition of a comprehensive bibliography ... by Franc D. Ingraham ... with the collaboration of Henry Swan ... Hannibal Hamlin ... John J. Lowrey ... [and others]
by Ingraham, Franc Douglas, 1898 and Children's Hospital (Boston, Mass.)
1944, 2,215,1
Encephalocele | Spina bifida | Bibliography
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8. Full Text Double encephalocele arising from single bone defect: A rare case
by Garg, Dileep and Singh, AdityaPratap and Tanger, Ramesh and Gupta, ArunK
Journal of Clinical Neonatology, ISSN 2249-4847, 2019, Volume 8, Issue 3, p. 176
Anencephaly | Encephalocele
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9. 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
The goals of this study were to report the clinical presentation, radiographic findings, operative strategy, and outcomes among patients with temporal bone... 
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
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10. Full Text Giant Parietal Encephalocele with Massive Brain Herniation and Suboccipital Encephalocele in a Neonate: An Unusual Form of Double Encephalocele
by Menekse, Guner and Celik, Haydar and Bayar, Mehmet Akif
World Neurosurgery, ISSN 1878-8750, 2016, Volume 98, pp. 867.e9 - 867.e11
Double encephalocele is extremely rare. We present an unusual form of double encephalocele including giant supratentorial and small infratentorial... 
Neurosurgery | Parietal | Encephalocele | Suboccipital | Double | SURGERY | OCCIPITAL ENCEPHALOCELE | CLINICAL NEUROLOGY | Magnetic Resonance Imaging | Encephalocele - congenital | Encephalocele - pathology | Rare Diseases - surgery | Humans | Rare Diseases - congenital | Female | Rare Diseases - pathology | Encephalocele - surgery | Parietal Lobe | Occipital Lobe | Infant, Newborn | Infants (Newborn)
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11. 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
Objectives/HypothesisTo describe our experience and current management approach for congenital nasal neuroglial heterotopia (NGH) and encephaloceles. Study... 
neuroglial heterotopia | encephalocele | Nasal glioma | congenital nasal lesion | Neuroglial heterotopia | Congenital nasal lesion | Encephalocele | MEDICINE, RESEARCH & EXPERIMENTAL | OTORHINOLARYNGOLOGY | 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
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12. Full Text Giant Interfrontal Encephalocele in an Infant: A Rare Entity
by Faheem, Mohd and Singh, Sunil Kumar and Ojha, Bal Krishna and Chandra, Anil and Srivastava, Chhitij and Jaiswal, Manish and Zeeshan, Qazi
Pediatric Neurosurgery, ISSN 1016-2291, 10/2016, Volume 51, Issue 6, pp. 309 - 312
Interfrontal encephalocele is one of the rare varieties of anterior encephalocele, and a giant interfrontal encephalocele is extremely rare. The authors could... 
Novel Insights from Clinical Practice | Giant interfrontal encephalocele | Infant | Anterior encephalocele | SURGERY | PEDIATRICS | OCCIPITAL ENCEPHALOCELE | ANTERIOR ENCEPHALOCELES | CLINICAL NEUROLOGY | Frontal Lobe - diagnostic imaging | Frontal Bone - diagnostic imaging | Frontal Bone - surgery | Frontal Lobe - surgery | Humans | Male | Rare Diseases | Encephalocele - diagnostic imaging | Encephalocele - surgery
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13. 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, ISSN 1018-4813, 06/2015, Volume 23, Issue 6, pp. 746 - 752
Meckel-Gruber Syndrome is a rare autosomal recessive lethal ciliopathy characterized by the triad of cystic renal dysplasia, occipital encephalocele and... 
SHH | ANOMALIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | PHENOTYPES | MUTATIONS | SPECTRUM | 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
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14. 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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15. Progressive skin necrosis of a huge occipital encephalocele
by Andarabi, Yasir and Nejat, Farideh and El-Khashab, Mostafa
10/2008
Objects: Progressive skin necrosis of giant occipital encephalocoele is an extremely rare complication found in neonates. Infection and ulceration of the... 
torsion | occipital encephalocele | Necrosis
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16. Full Text Repair of Frontoethmoidal Encephalocele in the Philippines: An account of 30 cases between 2008-2013
by Marshall, Amanda-Lynn, M.P.H and Setty, Pradeep, D.O and Hnatiuk, Mark, M.D and Pieper, Daniel R., M.D
World Neurosurgery, ISSN 1878-8750, 2017, Volume 103, pp. 19 - 27
Abstract Background Frontoethmoidal encephalocele is a congenital abnormality of the anterior skull base involving herniation of cranial contents through a... 
Neurosurgery | Pediatric craniofacial reconstruction | Skull base | Foramen cecum | Frontoethmoidal encephalocele | Neural tube defect | SURGERY | DIAGNOSIS | ENCEPHALOMENINGOCELE | MANAGEMENT | NASAL ENCEPHALOCELES | NEURAL-TUBE DEFECTS | CLINICAL NEUROLOGY | FUMONISINS | MENINGOENCEPHALOCELE | FOLATE | Frontal Bone - surgery | Oral and Maxillofacial Surgeons | Encephalocele - epidemiology | Humans | Child, Preschool | Patient Care Team | Infant | Male | Tomography, X-Ray Computed | Operative Time | Young Adult | Prefrontal Cortex - surgery | Medical Missions, Official | Ethmoid Bone - diagnostic imaging | Hydrocephalus - epidemiology | Adult | Female | Arachnoid Cysts - epidemiology | Child | Ethmoid Bone - surgery | Frontal Bone - diagnostic imaging | Comorbidity | Philippines | Nasal Bone - diagnostic imaging | Treatment Outcome | Postoperative Complications - epidemiology | Encephalocele - surgery | Neurosurgeons | Otolaryngologists | Surgery, Plastic | Arnold-Chiari Malformation - epidemiology | Nasal Bone - surgery | Adolescent | Encephalocele - diagnostic imaging | Prefrontal Cortex - diagnostic imaging | Reconstructive Surgical Procedures | Developing countries | Medical colleges | Encephalocele | Genetic disorders
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17. Full Text Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome
by Banin, Eyal and Badano, Jose L and Zaghloul, Norann A and Eyaid, Wafaa and Stoetzel, Corinne and Rix, Suzanne and Diaz-Font, Anna and Beales, Philip L and Katsanis, Nicholas and Alfadhel, Majid and Dollfus, Helene and Leitch, Carmen C and Davis, Erica E and Lewis, Richard Alan
Nature Genetics, ISSN 1061-4036, 04/2008, Volume 40, Issue 4, pp. 443 - 448
Meckel-Gruber syndrome (MKS) is a genetically heterogeneous, neonatally lethal malformation and the most common form of syndromic neural tube defect (NTD). To... 
JOUBERT-SYNDROME | DISRUPTION | DISSECTION | CILIUM | BBS LOCUS | GENETICS & HEREDITY | MKS3 | RPGRIP1L | MECKEL-GRUBER-SYNDROME | BASAL BODY PROTEIN | Embryo, Nonmammalian - cytology | Alternative Splicing | Humans | Embryo, Nonmammalian - metabolism | Child, Preschool | Molecular Sequence Data | Male | DNA Mutational Analysis | Bardet-Biedl Syndrome - pathology | Adult | Bardet-Biedl Syndrome - genetics | Female | Neoplasm Proteins - genetics | Child | Encephalocele - genetics | Amino Acid Sequence | Antigens, Neoplasm - genetics | Gastrulation | Membrane Proteins - genetics | Mutation - genetics | Zebrafish - growth & development | Syndrome | Zebrafish - genetics | Pregnancy | Proteins - genetics | Sequence Homology, Amino Acid | Homozygote | Animals | Pedigree | Zebrafish - metabolism | Usage | Gene mutations | Bardet-Biedl syndrome | Genetic aspects | Research | In situ hybridization | Health aspects | Risk factors | Proteins | Birth defects | Genetic disorders | Mutation | Molecular biology | Life Sciences | Bardet-Biedl Syndrome | Neoplasm Proteins | Genetics | Antigens, Neoplasm | Zebrafish | Membrane Proteins | Encephalocele | Embryo, Nonmammalian | Human genetics
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18. Full Text Secondary encephalocele in infant following subdural empyema repaired endoscopically-A case report
by Verma, Roshan K and Kaur, Navjot
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 09/2017, Volume 100, pp. 211 - 215
Subdural empyema (SDE) is an uncommon entity, mostly associated with meningitis and can be life threatening in infants. Rarely, a subdural empyema can lead to... 
Nasal encephalocele | Recurrent meningitis | Subdural empyema | Endoscopic repair | PEDIATRICS | OTORHINOLARYNGOLOGY | Meningitis - complications | Humans | Empyema, Subdural - complications | Infant | Male | Encephalocele - etiology | Encephalocele - surgery | Endoscopy | Encephalocele | Empyema | Meningitis
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19. Basal Encephalocele Associated with Teratoma; Pathogenesis and Management, Case Report
by Shahjouei, Shima and Nejat, Farideh and Khashab, El Mostafa
01/2014
Teratoma | Basal Encephalocele | Pathogenesis | Surgery | Hypertelorism
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20. Modern diagnosis and treatment in children with congenital basal encephalocele
by Sakharov, A.V and Roginskiy, V.V and Kapitanov, D.N and Ivanov, A.L and Shelesko, E.V and Gorelyshev, S.K and Evteev, A.A and Lemeneva, N.V and Zinkevich, D.N and Kochkin, Yu.A and Ozerova, V.I and Satanin, L.A
Zhurnal Voprosy Nejrokhirurgii Imeni N.N. Burdenko, ISSN 0042-8817, 2017, Volume 81, Issue 3, pp. 30 - 38
Encephalocele | Treatment | Basal encephalocele | Diagnosis | Congenital encephalocele
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