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1. Full Text Fetal evaluation of spine dysraphism
by Bulas, Dorothy
Pediatric radiology, ISSN 0301-0449, 6/2010, Volume 40, Issue 6, pp. 1029 - 1037
Pediatrics | Medicine & Public Health | MRI | Dysraphism | Oncology | Fetal | Nuclear Medicine | Imaging / Radiology | Ultrasound | Neuroradiology | Diagnostic Imaging - methods | Spinal Dysraphism - diagnosis | Prenatal Diagnosis - methods | Humans | Spina bifida | Care and treatment | Usage | Diagnostic imaging | Genetic disorders | Diagnosis | Vitamin B | Birth defects | Three dimensional imaging | Index Medicus
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2. Full Text Genetic analysis of spinal dysraphism with a hamartomatous growth (appendix) of the spinal cord: a case series
by Bartels, R.H.M.A and Grotenhuis, J.A and Stegmann, A.P.A and Brunner, H.G
BMC neurology, ISSN 1471-2377, 2020, Volume 20, Issue 1, pp. 121 - 121
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Spinal Cord - abnormalities | Hamartoma - genetics | Humans | Middle Aged | Spinal Dysraphism - genetics | Neural Tube Defects - genetics | Adult | Female | Male | Hamartoma - complications | Appendix | Spinal cord | Congenital diseases | Pathogenesis | Congenital defects | Neural tube defects | Genes | Heredity | Genomes | Patients | Defects | Genetic variance | Hypotheses | Neural tube | Magnetic resonance imaging | Genetic analysis | Index Medicus | Case series | Abnormal development
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3. Full Text Complex forms of spinal dysraphism
by Patnaik, Ashis and Mahapatra, Ashok Kumar
Child's nervous system, ISSN 0256-7040, 9/2013, Volume 29, Issue 9, pp. 1527 - 1532
Spina bifida | Neurosciences | Medicine & Public Health | Spinal lipoma | Neurenteric cyst | Neurosurgery | Split cord malformation | Complex spinal dysraphism | Pediatrics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Surgery | Science & Technology | Spinal Cord - abnormalities | Spinal Cord - embryology | Spinal Dysraphism - diagnosis | Humans | Care and treatment | Genetic aspects | Prognosis | Research | Risk factors | Index Medicus | Congenital defects
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4. Full Text Decreased rectal meconium signal on MRI in fetuses with open spinal dysraphism
by Nagaraj, Usha D and Calvo‐Garcia, Maria A and Merrow, Arnold C and Zhang, Bin and Kline‐Fath, Beth M
Prenatal diagnosis, ISSN 0197-3851, 10/2018, Volume 38, Issue 11, pp. 870 - 875
Genetics & Heredity | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Magnetic resonance imaging | Analysis | Health insurance industry | Neonates | Spinal cord | Medical imaging | Congenital defects | Fetuses | Neural tube defects | Bladder | Prenatal development | Anorectal | Gestational age | Anus | Intestine | Rectum | Meconium | Diagnostic systems | Age | Index Medicus
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5. Full Text The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation
by Kousa, Youssef A and Zhu, Huiping and Fakhouri, Walid D and Lei, Yunping and Kinoshita, Akira and Roushangar, Raeuf R and Patel, Nicole K and Agopian, A J and Yang, Wei and Leslie, Elizabeth J and Busch, Tamara D and Mansour, Tamer A and Li, Xiao and Smith, Arianna L and Li, Edward B and Sharma, Dhruv B and Williams, Trevor J and Chai, Yang and Amendt, Brad A and Liao, Eric C and Mitchell, Laura E and Bassuk, Alexander G and Gregory, Simon and Ashley-Koch, Allison and Shaw, Gary M and Finnell, Richard H and Schutte, Brian C
Human molecular genetics, ISSN 0964-6906, 05/2019, Volume 28, Issue 10, pp. 1726 - 1737
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Conserved Sequence - genetics | Spinal Dysraphism - pathology | Humans | Spinal Dysraphism - genetics | Neural Tube Defects - genetics | Gene Expression Regulation, Developmental - genetics | Interferon Regulatory Factors - genetics | Neural Tube Defects - pathology | Signal Transduction - genetics | Neurulation - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Neural Tube - pathology | Transcription Factor AP-2 - genetics | Animals | Mice | Mutation | Neural Tube - growth & development | Index Medicus | General
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6. Full Text Congenital spine anomalies: the closed spinal dysraphisms
by Schwartz, Erin Simon and Rossi, Andrea
Pediatric radiology, ISSN 0301-0449, 9/2015, Volume 45, Issue S3, pp. 413 - 419
Pediatrics | Medicine & Public Health | Magnetic resonance imaging | Spine | Dysraphism | Oncology | Anomaly | Nuclear Medicine | Children | Imaging / Radiology | Ultrasound | Neuroradiology | Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Spine - abnormalities | Spinal Dysraphism - pathology | Humans | Magnetic Resonance Imaging - methods | Neural Tube Defects - pathology | Female | Male | Image Enhancement - methods | Spine - pathology | Infant, Newborn | Genetic disorders | Dysmorphology | Diagnosis | Research | Index Medicus
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7. Full Text Currarino syndrome and spinal dysraphism
by Kole, Matthew J and Fridley, Jared S and Jea, Andrew and Bollo, Robert J
Journal of neurosurgery. Pediatrics, 06/2014, Volume 13, Issue 6, pp. 685 - 689
Meningomyelocele - surgery | Humans | Lipoma - surgery | Infant | Male | Sacrum - abnormalities | Digestive System Abnormalities - surgery | Abnormalities, Multiple - surgery | Meningomyelocele - diagnosis | Spinal Dysraphism - diagnosis | Sacrum - surgery | Spinal Cord Neoplasms - surgery | Rectum - surgery | Abnormalities, Multiple - genetics | Infant, Newborn | Syringomyelia - diagnosis | Syringomyelia - surgery | Neural Tube Defects - surgery | Transcription Factors - genetics | Homeodomain Proteins - genetics | Rectum - abnormalities | Anal Canal - abnormalities | Digestive System Abnormalities - diagnosis | Magnetic Resonance Imaging | Neural Tube Defects - diagnosis | Abnormalities, Multiple - diagnosis | Spinal Cord Neoplasms - diagnosis | Anal Canal - surgery | Lipoma - diagnosis | Spinal Dysraphism - surgery | Index Medicus
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8. Full Text Sprengel's deformity and spinal dysraphism: connecting the shoulder and the spine
by van Aalst, J and Vles, J. S. H and Cuppen, I and Sival, D. A and Niks, E. H and Van Rhijn, L. W and Van Steensel, M. A. M and Cornips, E. M. J
Child's nervous system, ISSN 0256-7040, 07/2013, Volume 29, Issue 7, pp. 1051 - 1058
Spondylocostal dysostosis | DYSOSTOSIS | MANAGEMENT | KLIPPEL-FEIL-SYNDROME | MECHANISM | Spinal dysraphism | ANOMALIES | NEURAL-TUBE DEFECTS | SPLIT CORD MALFORMATION | DYSPLASIA | Jarcho-Levin syndrome | Spina bifida | Embryology | SCAPULA | SEGMENTATION | Genetics | Neurosciences | Medicine & Public Health | Neurosurgery | Jarcho–Levin syndrome | Pediatrics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Surgery | Science & Technology | Humans | Child, Preschool | Infant | Male | Tomography, X-Ray Computed | Abnormalities, Multiple - embryology | Clubfoot | Congenital Abnormalities - diagnosis | Netherlands | Spinal Dysraphism - diagnosis | Shoulder Joint - abnormalities | Female | Spine - embryology | Shoulder - embryology | Spinal Dysraphism - embryology | Meningomyelocele | Child | Infant, Newborn | Scapula - embryology | Scapula - abnormalities | Congenital Abnormalities - embryology | Magnetic Resonance Imaging | Hemangioma | Syringomyelia | Shoulder Joint - embryology | Abnormalities, Multiple - diagnosis | Skin Neoplasms | Care and treatment | Diagnosis | Research | Risk factors | Index Medicus
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9. Full Text Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice
by De Castro, Sandra C P and Gustavsson, Peter and Marshall, Abigail R and Gordon, William M and Galea, Gabriel and Nikolopoulou, Evanthia and Savery, Dawn and Rolo, Ana and Stanier, Philip and Andersen, Bogi and Copp, Andrew J and Greene, Nicholas D E
Human molecular genetics, ISSN 0964-6906, 12/2018, Volume 27, Issue 24, pp. 4218 - 4230
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Spinal Dysraphism - pathology | Loss of Function Mutation | Humans | Spinal Dysraphism - genetics | Embryonic Development - genetics | Neural Tube Defects - genetics | Gene Expression Regulation, Developmental - genetics | Neural Tube Defects - pathology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Animals | Animals, Genetically Modified - genetics | Alleles | Protein Multimerization - genetics | Mice | Disease Models, Animal | Index Medicus | General
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10. Full Text Non-neural surface ectodermal rosette formation and F-actin dynamics drive mammalian neural tube closure
by Zhou, Chengji J and Ji, Yu and Reynolds, Kurt and McMahon, Moira and Garland, Michael A and Zhang, Shuwen and Sun, Bo and Gu, Ran and Islam, Mohammad and Liu, Yue and Zhao, Tianyu and Hsu, Grace and Iwasa, Janet
Biochemical and biophysical research communications, ISSN 0006-291X, 06/2020, Volume 526, Issue 3, pp. 647 - 653
Multicellular rosette formation | Non-neural surface ectodermal cells | Posterior neuropore (PNP) | Convergent F-actin protrusions and cable network | Grhl3-KO mice | Computational visual modeling | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Ectoderm - embryology | Ectoderm - ultrastructure | Neural Tube Defects - embryology | Spinal Dysraphism - genetics | Actins - metabolism | Neural Tube Defects - genetics | Spine - metabolism | Neural Tube Defects - metabolism | Neurulation | Ectoderm - abnormalities | Spine - abnormalities | Ectoderm - metabolism | Actins - analysis | Neural Tube - metabolism | Spine - embryology | Spinal Dysraphism - embryology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Animals | Spine - ultrastructure | Neural Tube - ultrastructure | Mice | Spinal Dysraphism - metabolism | Mutation | Neural Tube - embryology | Neural Tube - abnormalities | Index Medicus
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11. Full Text Epidemiologic and genetic aspects of spina bifida and other neural tube defects
by Au, Kit Sing and Ashley‐Koch, Allison and Northrup, Hope
Developmental disabilities research reviews, ISSN 1940-5510, 2010, Volume 16, Issue 1, pp. 6 - 15
epidemiology | neural tube defects | genetic association studies | meningomyleocele | spina bifida | Meningomyleocele | Genetic association studies | Spina bifida | Epidemiology | Neural tube defects | Pediatrics | Neurosciences | Clinical Neurology | Life Sciences & Biomedicine | Neurosciences & Neurology | Psychiatry | Science & Technology | Neurological Impairments | Nutrition | Congenital Impairments | Age Differences | Prenatal Influences | Parents | Socioeconomic Status | Disabilities | Risk | Racial Differences | Metabolism | Employment Level | Pregnancy | Prevention | Etiology | Genetics | Drug Use | Meningomyelocele - epidemiology | Folic Acid Deficiency - metabolism | Humans | Spinal Dysraphism - genetics | Neural Tube Defects - genetics | Folic Acid Deficiency - epidemiology | Neural Tube Defects - metabolism | Fever - epidemiology | Pregnancy Trimester, First | Meningomyelocele - metabolism | Socioeconomic Factors | Female | Vitamin B 12 Deficiency - epidemiology | Vitamin B 12 Deficiency - metabolism | Ethnic Groups - statistics & numerical data | Gene Expression | Genome-Wide Association Study | Birth Order | Prenatal Diagnosis | Neural Tube Defects - epidemiology | Genotype | Phenotype | Meningomyelocele - genetics | Spinal Dysraphism - epidemiology | Glucose - metabolism | Spinal Dysraphism - metabolism | Pregnancy Complications - epidemiology | Index Medicus
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