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Journal Article
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC, ISSN 1701-2163, 07/2019
Encephalocele, a rare congenital brain malformation, is herniation of brain tissue with or without meninges through a cranial fossa defect. It is classified by... 
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 06/2015, Volume 23, Issue 6, pp. 746 - 752
Journal Article
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 09/2017, Volume 50, Issue S1, pp. 263 - 263
Journal Article
Current opinion in otolaryngology & head and neck surgery, ISSN 1068-9508, 10/2019, Volume 27, Issue 5, pp. 369 - 375
To describe the current state in the diagnosis and management of spontaneous cerebrospinal fluid (sCSF) fistula and encephaloceles. The increased incidence of... 
Encephalocele | Care and treatment | Central nervous system diseases | Fistula | Cerebrospinal fluid | Diagnosis | Health aspects | Index Medicus
Journal Article
Acta Neurochirurgica, ISSN 0001-6268, 3/2013, Volume 155, Issue 3, pp. 495 - 496
Neurology | Surgical Orthopedics | Medicine & Public Health | Minimally Invasive Surgery | Neurosurgery | Interventional Radiology | Neuroradiology | SURGERY | PITUITARY-TUMORS | MACROPROLACTINOMA | THERAPY | MANAGEMENT | CHIASMAL HERNIATION | COMPLICATION | BROMOCRIPTINE | CLINICAL NEUROLOGY | Neoplasm, Residual - pathology | Pituitary Neoplasms - surgery | Optic Nerve - pathology | Pituitary Neoplasms - diagnosis | Humans | Optic Nerve Diseases - diagnosis | Dopamine Agonists - therapeutic use | Male | Dopamine Agonists - adverse effects | Nerve Compression Syndromes - chemically induced | Visual Fields - drug effects | Tissue Adhesions - chemically induced | Tissue Adhesions - surgery | Nerve Degeneration - chemically induced | Empty Sella Syndrome - chemically induced | Neoplasm, Residual - diagnosis | Nerve Compression Syndromes - diagnosis | Blindness - surgery | Hernia - diagnosis | Nerve Degeneration - diagnosis | Prolactinoma - drug therapy | Prolactinoma - surgery | Blindness - chemically induced | Postoperative Complications - pathology | Nerve Compression Syndromes - surgery | Optic Chiasm - surgery | Encephalocele - diagnosis | Optic Nerve Diseases - chemically induced | Empty Sella Syndrome - surgery | Nerve Degeneration - surgery | Blindness - diagnosis | Encephalocele - chemically induced | Encephalocele - surgery | Optic Nerve Diseases - surgery | Postoperative Complications - diagnosis | Hernia - chemically induced | Prolactinoma - diagnosis | Magnetic Resonance Imaging | Empty Sella Syndrome - diagnosis | Frontal Lobe - surgery | Pituitary Neoplasms - drug therapy | Frontal Lobe - drug effects | Optic Nerve - surgery | Tissue Adhesions - diagnosis | Craniotomy | Optic Chiasm - pathology | Frontal Lobe - pathology | Optic Chiasm - drug effects
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 1/2016, Volume 31, Issue 1, pp. 113 - 119
Hepatorenal fibrocystic diseases (HRFCDs) are a group of monogenic disorders characterized by developmental abnormalities involving the liver and kidney. In... 
Pediatrics | Autosomal-recessive polycystic kidney disease | Ciliopathy | Nephrology | Nephronophthisis 13 | Medicine & Public Health | Congenital hepatic fibrosis | Caroli disease | Urology | Hepatorenal fibrocystic disease | GENOTYPE-PHENOTYPE CORRELATION | DIAGNOSIS | MANAGEMENT | CILIOPATHIES | POLYCYSTIC KIDNEY-DISEASE | DISORDERS | MECHANISMS | LIVER-DISEASE | CILIA | PATHOGENESIS | UROLOGY & NEPHROLOGY | PEDIATRICS | Polycystic Kidney Diseases - genetics | Predictive Value of Tests | Polycystic Kidney Diseases - diagnosis | Genetic Testing | Prognosis | Age Factors | Encephalocele - epidemiology | Humans | Genetic Diseases, Inborn - genetics | Child, Preschool | Caroli Disease - diagnosis | Infant | Male | Genetic Diseases, Inborn - epidemiology | Polycystic Kidney, Autosomal Recessive - diagnosis | Caroli Disease - genetics | Polycystic Kidney, Autosomal Recessive - genetics | Liver Cirrhosis - epidemiology | Renal Insufficiency, Chronic - epidemiology | Young Adult | Caroli Disease - epidemiology | Adult | Female | Republic of Korea - epidemiology | Child | Genetic Diseases, Inborn - diagnosis | Liver Cirrhosis - genetics | Encephalocele - genetics | Ciliary Motility Disorders - epidemiology | Encephalocele - diagnosis | Genetic Predisposition to Disease | Liver Cirrhosis - diagnosis | Risk Factors | Polycystic Kidney, Autosomal Recessive - epidemiology | Phenotype | Kidney Failure, Chronic - epidemiology | Adolescent | Ciliary Motility Disorders - diagnosis | Polycystic Kidney Diseases - epidemiology | Ciliary Motility Disorders - genetics | Index Medicus
Journal Article
The Journal of craniofacial surgery, ISSN 1049-2275, 2010, Volume 21, Issue 5, pp. 1581 - 1582
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 07/2016, Volume 134, Issue 7, pp. 753 - 762
Journal Article
by Travaglini, Lorena and Brancati, Francesco and Silhavy, Jennifer and Iannicelli, Miriam and Nickerson, Elizabeth and Elkhartoufi, Nadia and Scott, Eric and Spencer, Emily and Gabriel, Stacey and Thomas, Sophie and Ben-Zeev, Bruria and Bertini, Enrico and Boltshauser, Eugen and Chaouch, Malika and Cilio, Maria Roberta and de Jong, Mirjam M and Kayserili, Hulya and Ogur, Gonul and Poretti, Anea and Signorini, Sabrina and Uziel, Graziella and Zaki, Maha S and Johnson, Colin and Attié-Bitach, Tania and Gleeson, Joseph G and Valente, Enza Maria and Ali Pacha, L and Zankl, A and Leventer, R and Grattan-Smith, P and Janecke, A and Koch, J and Freilinger, M and D'Hooghe, M and Sznajer, Y and Vilain, C and van Coster, R and Demerleir, L and Dias, K and Moco, C and Moreira, A and Ae Kim, C and Maegawa, G and Dakovic, I and Loncarevic, D and Mejaski-Bosnjak, V and Petkovic, D and Abdel-Salam, G. M. H and Abdel-Aleem, A and Marti, I and Pinard, J. M and Quijano-Roy, S and Sigaudy, S and de Lonlay, P and Romano, S and Verloes, A and Touraine, R and Koenig, M and Dollfus, H and Flori, E and Fradin, M and Lagier-Tourenne, C and Messer, J and Collignon, P and Penzien, J. M and Bussmann, C and Merkenschlager, A and Philippi, H and Kurlemann, G and Grundmann, K and Dacou-Voutetakis, C and Kitsiou Tzeli, S and Pons, R and Jerney, J and Halldorsson, S and Johannsdottir, J and Ludvigsson, P and Phadke, S. R and Girisha, K. M and Doshi, H and Udani, V and Kaul, M and Stuart, B and Magee, A and Spiegel, R and Shalev, S and Mandel, H and Lev, D and Michelson, M and Idit, M and Ben-Zeev, B and Gershoni-Baruch, R and Ficcadenti, A and Fischetto, R and Gentile, M and Della Monica, M and Pezzani, M and Graziano, C and Seri, M and Benedicenti, F and ... and Int JSRD Study Grp and International JSRD Study Group and the International JSRD Study Group
European journal of human genetics, ISSN 1018-4813, 2013, Volume 21, Issue 10, pp. 1074 - 1078
Journal Article