All Relations between Spinal Dysraphism and spinal cord

Publication Sentence Publish Date Extraction Date Species
Noritoshi Sekid. Editorial Comment to 31-year follow-up of those with occult spinal dysraphism who underwent spinal cord untethering: Lower urinary tract function, skin stigmata, fertility, and work participation. International journal of urology : official journal of the Japanese Urological Association. 2024-05-02. PMID:38693659. editorial comment to 31-year follow-up of those with occult spinal dysraphism who underwent spinal cord untethering: lower urinary tract function, skin stigmata, fertility, and work participation. 2024-05-02 2024-05-04 Not clear
Atsuo Kondo, Osamu Kamihira, Tomonori Itoh, Momokazu Gotoh, Kumiko Kat. A 31-year follow-up of those with occult spinal dysraphism, who underwent spinal cord untethering: Lower urinary tract function, skin stigmata, fertility, and work participation. International journal of urology : official journal of the Japanese Urological Association. 2024-04-18. PMID:38634346. a 31-year follow-up of those with occult spinal dysraphism, who underwent spinal cord untethering: lower urinary tract function, skin stigmata, fertility, and work participation. 2024-04-18 2024-04-20 Not clear
Atsuo Kondo, Osamu Kamihira, Tomonori Itoh, Momokazu Gotoh, Kumiko Kat. A 31-year follow-up of those with occult spinal dysraphism, who underwent spinal cord untethering: Lower urinary tract function, skin stigmata, fertility, and work participation. International journal of urology : official journal of the Japanese Urological Association. 2024-04-18. PMID:38634346. this study evaluated patients with occult spinal dysraphism who underwent spinal cord untethering. 2024-04-18 2024-04-20 Not clear
Peter Spazzapan, Tomaz Velnar, Nina Perosa, Andrej Porcnik, Borut Presto. Results of Surgical Treatment of Occult Spinal Dysraphisms-A Single Centre Experience. Diagnostics (Basel, Switzerland). vol 14. issue 7. 2024-04-13. PMID:38611616. occult spinal dysraphisms (osds) are caused by various defects in the embryogenesis of the spinal cord and represent an obstacle to the ascent of the conus, which allows the conus to pass from the lower levels of the spinal canal to the final position between l1 and l2 during normal foetal life. 2024-04-13 2024-04-15 Not clear
Mohit K Shrivastva, Mousam Panigrah. Imaging spectrum of spinal dysraphism: A diagnostic challenge. SA journal of radiology. vol 27. issue 1. 2024-02-22. PMID:38384981. spinal dysraphism (sd) is a collective term for congenital malformations of the spine and spinal cord. 2024-02-22 2024-02-24 Not clear
Hidekazu Aoki, Shunji Mugikura, Reizo Shirane, Toshiaki Hayashi, Tomomi Kimiwada, Kiyohide Sakai, Keiko Ainoya, Hideki Ota, Kei Takase, Yoshihisa Shimanuk. Role of Magnetic Resonance Imaging in the Screening of Closed Spinal Dysraphism. Neurologia medico-chirurgica. 2023-08-30. PMID:37648539. closed spinal dysraphism (csd) encompasses a heterogeneous group of spinal cord deformities, which can be accompanied by several types of skin stigmata. 2023-08-30 2023-09-07 Not clear
Kwanjin Par. Urological Aspects of Spinal Dysraphism. Advances and technical standards in neurosurgery. vol 47. 2023-08-28. PMID:37640879. however, the diagnosis of neurogenic bladder in those with spinal dysraphism is often difficult and contrasted to other types of neurogenic bladder caused by complete neural lesions such as spinal cord injury or brain tumor. 2023-08-28 2023-09-07 Not clear
Zubair Tahir, Claudia Crave. Gastrulation and Split Cord Malformation. Advances and technical standards in neurosurgery. vol 47. 2023-08-28. PMID:37640870. split cord malformation (scm) is a rare form of closed spinal dysraphism, in which two hemi-cords are present, instead of a single spinal cord. 2023-08-28 2023-09-07 Not clear
Claudia Pasquali, Federica Basaldella, Francesco Sal. Updates on Intraoperative Neurophysiology During Surgery for Spinal Dysraphism. Advances and technical standards in neurosurgery. vol 47. 2023-08-28. PMID:37640878. spinal dysraphism is a group of disorders resulting from an embryologic failure of spinal cord development which can lead to a radicular-medullary mechanical stretch that generates vascular compromise and hypoxic-ischemic damage to the nervous structures of the conus-cauda region.thus, the clinical relevance of the different types of spinal dysraphism is related to the possible neurologic deficits resulting from spinal cord tethering. 2023-08-28 2023-09-07 human
Britta L Bureau, Eileen Sherburne, John G Thometz, Andrew B Fo. Prophylactic spinal cord untethering in children with spinal dysraphism undergoing thoracolumbar fusion for scoliosis. World neurosurgery. 2023-07-27. PMID:37499752. prophylactic spinal cord untethering in children with spinal dysraphism undergoing thoracolumbar fusion for scoliosis. 2023-07-27 2023-08-14 Not clear
Britta L Bureau, Eileen Sherburne, John G Thometz, Andrew B Fo. Prophylactic spinal cord untethering in children with spinal dysraphism undergoing thoracolumbar fusion for scoliosis. World neurosurgery. 2023-07-27. PMID:37499752. it remains unclear whether spinal cord untethering is necessary to reduce the chances of neurologic decline in children with myelomeningocele and complex closed spinal dysraphism who undergo thoracolumbar fusion for scoliosis. 2023-07-27 2023-08-14 Not clear
Britta L Bureau, Eileen Sherburne, John G Thometz, Andrew B Fo. Prophylactic spinal cord untethering in children with spinal dysraphism undergoing thoracolumbar fusion for scoliosis. World neurosurgery. 2023-07-27. PMID:37499752. we sought to determine the neurologic and functional outcomes of children with spinal dysraphism undergoing spinal fusion for scoliosis with and without prophylactic spinal cord untethering. 2023-07-27 2023-08-14 Not clear
Paula Arbelo-Pérez, Tania de Ganzo-Suárez, José Fernando de Luis-Escuder. Prenatal Diagnosis of Diastematomyelia: a Case Report and Literature Review. Reproductive sciences (Thousand Oaks, Calif.). 2023-07-25. PMID:37491555. diastematomyelia is a type of closed spinal dysraphism in which there is splitting of the spinal cord. 2023-07-25 2023-08-14 Not clear
Chun-Ming Lin, Michael Oglesbee, David Knudsen, Thomas W Smit. Ischemic myelomalacia and closed spinal dysraphism in multiple finishing swine. Veterinary pathology. 2022-12-16. PMID:36524748. on the other hand, congenital spinal cord malformations result from neural tube defects in fetal development (ie, spinal dysraphism), with structural anomalies referred to collectively as myelodysplasia. 2022-12-16 2023-08-14 Not clear
Wai Cheong Soon, Joe M Das, Azam Baig, Pasquale Gallo, Desiderio Rodrigues, William B L. Atlantoaxial limited dorsal myeloschisis: A report of two cases and review of literature. Brain & spine. vol 1. 2022-10-17. PMID:36247398. limited dorsal myeloschisis (ldm) is a rare form of spinal dysraphism that is characterised by a distinctive fibroneural stalk connecting the spinal cord to the overlying skin lesion. 2022-10-17 2023-08-14 Not clear
Christina White, Sarah Sarvis Milla, John A Maloney, Ilana Neuberge. Imaging of Congenital Spine Malformations. Clinics in perinatology. vol 49. issue 3. 2022-09-16. PMID:36113926. congenital malformations of the spine and spinal cord are a large and diverse group of diagnoses, which are often broadly referred to as spinal dysraphisms (sds). 2022-09-16 2023-08-14 Not clear
Ahmed Harazeen, Neeharika Thottempudi, Joseph Sonstein, Xiangping Li, Laura Wu, Prashant Rai, Todd Mase. Tethered Cord Syndrome Associated With Lumbar Lipomyelomeningocele: A Case Report. Cureus. vol 14. issue 2. 2022-03-31. PMID:35355549. lipomyelomeningocele is a type of closed spinal dysraphism typically presenting as a lipomatous mass contiguous with a neural defect above the gluteal crease. tethered cord syndrome is defined as symptoms and signs caused by excessive spinal cord tension from an abnormally low conus medullaris, with an abnormally thick filum terminale attached to the lower sacral region. a 19-year-old male with no remarkable medical history presented with low back pain and urinary incontinence for the past one year. 2022-03-31 2023-08-13 Not clear
Nobuya Murakami, Ai Kurogi, Yoshihisa Kawakami, Yushi Noguchi, Makoto Hayashida, Satoshi O Suzuki, Nobutaka Mukae, Takafumi Shimogawa, Koji Yoshimoto, Takato Moriok. Refractory CSF leakage following untethering surgery performed 10 months after birth for enlarging terminal myelocystocele associated with OEIS complex. Surgical neurology international. vol 12. 2022-03-30. PMID:35350825. terminal myelocystocele (tmc) is an occult spinal dysraphism characterized by cystic dilatation of the terminal spinal cord in the shape of a trumpet (myelocystocele) filled with cerebrospinal fluid (csf), which herniates into the extraspinal subcutaneous region. 2022-03-30 2023-08-13 Not clear
Gesa Cohrs, Ann-Kathrin Blumenröther, Jan-Philip Sürie, Michael Synowitz, Janka Held-Feindt, Friederike Knerlich-Lukoschu. Fetal and Perinatal Expression Profiles of Proinflammatory Cytokines in the Neuroplacodes of Rats with Myelomeningoceles: A Contribution to the Understanding of Secondary Spinal Cord Injury in Open Spinal Dysraphism. Journal of neurotrauma. 2021-11-29. PMID:34541905. fetal and perinatal expression profiles of proinflammatory cytokines in the neuroplacodes of rats with myelomeningoceles: a contribution to the understanding of secondary spinal cord injury in open spinal dysraphism. 2021-11-29 2023-08-13 human
Bárbara Trapp, Tomás de Andrade Lourenção Freddi, Monique de Oliveira Morais Hans, Isadora Fonseca Teixeira Lemos Calixto, Emi Fujino, Laila Cristina Alves Rojas, Stênio Burlin, Danilo Manuel Cerqueira Costa, Henrique Carrete Junior, Nitamar Abdala, Luís Antônio Tobaru Tibana, Eduardo Takashi Takehara, Gustavo Dalul Gome. A Practical Approach to Diagnosis of Spinal Dysraphism. Radiographics : a review publication of the Radiological Society of North America, Inc. vol 41. issue 2. 2021-11-24. PMID:33449837. spinal dysraphisms (sds) are congenital malformations of the spinal cord, determined by derangement in the complex cascade of embryologic events involved in spinal development. 2021-11-24 2023-08-13 Not clear