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1987 5
1988 5
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1990 9
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1994 17
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2001 25
2002 27
2003 24
2004 18
2005 27
2006 24
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2013 35
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Your search for SERKAL syndrome AND humans[mesh] AND review[publication type] retrieved no results
Non-IgE-Mediated Gastrointestinal Food Allergies in Children: An Update.
Labrosse R, Graham F, Caubet JC. Labrosse R, et al. Nutrients. 2020 Jul 14;12(7):2086. doi: 10.3390/nu12072086. Nutrients. 2020. PMID: 32674427 Free PMC article. Review.
Non-immunoglobulin E-mediated gastrointestinal food allergic disorders (non-IgE-GI-FA) include food protein-induced enterocolitis syndrome (FPIES), food protein-induced enteropathy (FPE) and food protein-induced allergic proctocolitis (FPIAP), which present with symptoms o …
Non-immunoglobulin E-mediated gastrointestinal food allergic disorders (non-IgE-GI-FA) include food protein-induced enterocolitis syndrom
Axonal variants of Guillain-Barre syndrome: an update.
Shang P, Zhu M, Wang Y, Zheng X, Wu X, Zhu J, Feng J, Zhang HL. Shang P, et al. J Neurol. 2021 Jul;268(7):2402-2419. doi: 10.1007/s00415-020-09742-2. Epub 2020 Mar 5. J Neurol. 2021. PMID: 32140865 Review.
Axonal variants of Guillain-Barre syndrome (GBS) mainly include acute motor axonal neuropathy, acute motor and sensory axonal neuropathy, and pharyngeal-cervical-brachial weakness. ...However, the pathogenetic mechanisms of axonal GBS related to antecedent bacterial or vir …
Axonal variants of Guillain-Barre syndrome (GBS) mainly include acute motor axonal neuropathy, acute motor and sensory axonal neuropa …
Update on twin-to-twin transfusion syndrome.
Bamberg C, Hecher K. Bamberg C, et al. Best Pract Res Clin Obstet Gynaecol. 2019 Jul;58:55-65. doi: 10.1016/j.bpobgyn.2018.12.011. Epub 2019 Jan 5. Best Pract Res Clin Obstet Gynaecol. 2019. PMID: 30850326 Review.
Twin-to-twin transfusion syndrome (TTTS) is a serious complication that affects 10-15% of monochorionic multiple pregnancies. ...There is evidence for the superiority of fetoscopic laser ablation over serial amnioreductions regarding survival and neurological outcom …
Twin-to-twin transfusion syndrome (TTTS) is a serious complication that affects 10-15% of monochorionic multiple pregnancies. ...Ther …
Chronic Pericardial Effusion: Causes and Management.
Lazaros G, Imazio M, Tsioufis P, Lazarou E, Vlachopoulos C, Tsioufis C. Lazaros G, et al. Can J Cardiol. 2023 Aug;39(8):1121-1131. doi: 10.1016/j.cjca.2023.02.003. Epub 2023 Feb 10. Can J Cardiol. 2023. PMID: 36773704 Review.
Chronic pericardial effusion is a common pericardial syndrome whose approach has been well standardised in recent years. ...Among investigations used during diagnostic work-up, echocardiography is of paramount importance for the diagnosis, sizing, and serial evaluat …
Chronic pericardial effusion is a common pericardial syndrome whose approach has been well standardised in recent years. ...Among inv …
Twin-to-twin transfusion syndrome: Controversies in the diagnosis and management.
Bamberg C, Hecher K. Bamberg C, et al. Best Pract Res Clin Obstet Gynaecol. 2022 Nov;84:143-154. doi: 10.1016/j.bpobgyn.2022.03.013. Epub 2022 Mar 30. Best Pract Res Clin Obstet Gynaecol. 2022. PMID: 35589537 Review.
In twin-to-twin transfusion syndrome (TTTS) communicating placental vessels on the chorionic plate between the donor and recipient twins are responsible for the chronic imbalance of blood flow. Evidence demonstrates that fetoscopic laser ablation is superior to serial
In twin-to-twin transfusion syndrome (TTTS) communicating placental vessels on the chorionic plate between the donor and recipient tw …
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis.
Farncombe KM, Thain E, Barnett-Tapia C, Sadeghian H, Kim RH. Farncombe KM, et al. BMC Med Genomics. 2022 Jul 15;15(1):160. doi: 10.1186/s12920-022-01304-x. BMC Med Genomics. 2022. PMID: 35840934 Free PMC article. Review.
BACKGROUND: Noonan syndrome (NS) is a genetic disorder characterized by developmental delays, typical facial gestalt and cardiovascular defects. ...Whole exome sequencing at age 23 identified a novel de novo likely pathogenic heterozygous variant in the LZTR1 gene denoted …
BACKGROUND: Noonan syndrome (NS) is a genetic disorder characterized by developmental delays, typical facial gestalt and cardiovascul …
Optimizing Treatment for Adults with HIV/AIDS in China: Successes over Two Decades and Remaining Challenges.
Cao W, Hsieh E, Li T. Cao W, et al. Curr HIV/AIDS Rep. 2020 Feb;17(1):26-34. doi: 10.1007/s11904-019-00478-x. Curr HIV/AIDS Rep. 2020. PMID: 31939111 Free PMC article. Review.
RECENT FINDINGS: Continuous optimization of the Chinese National Guidelines for HIV/AIDS Diagnosis and Treatment has been guided by data from serial domestic multi-center studies aimed at evaluating efficacy and toxicity of available ART regimens among Chinese patients wit …
RECENT FINDINGS: Continuous optimization of the Chinese National Guidelines for HIV/AIDS Diagnosis and Treatment has been guided by data fro …
Sensory Neuronopathies.
Crowell A, Gwathmey KG. Crowell A, et al. Curr Neurol Neurosci Rep. 2017 Aug 23;17(10):79. doi: 10.1007/s11910-017-0784-4. Curr Neurol Neurosci Rep. 2017. PMID: 28836102 Review.
RECENT FINDINGS: Diagnostic criteria have recently been published and validated to allow differentiation of sensory neuronopathies from other polyneuropathies. On the basis of serial electrodiagnostic studies, the treatment window for the acquired sensory neuronopathies ha …
RECENT FINDINGS: Diagnostic criteria have recently been published and validated to allow differentiation of sensory neuronopathies from othe …
Saliva biomarkers in oral disease.
Zhou Y, Liu Z. Zhou Y, et al. Clin Chim Acta. 2023 Aug 1;548:117503. doi: 10.1016/j.cca.2023.117503. Epub 2023 Aug 2. Clin Chim Acta. 2023. PMID: 37536520 Review.
Saliva collection is noninvasive and highly applicable for tests requiring serial sampling. Furthermore, advances in test accuracy, sensitivity and precision for saliva has improved diagnostic performance as well as the identification of novel markers especially in oral di …
Saliva collection is noninvasive and highly applicable for tests requiring serial sampling. Furthermore, advances in test accuracy, s …
Why Would a Child Have a Stroke?
Persa L, Shaw DW, Amlie-Lefond C. Persa L, et al. J Child Neurol. 2022 Dec;37(12-14):907-915. doi: 10.1177/08830738221129916. Epub 2022 Oct 9. J Child Neurol. 2022. PMID: 36214173 Review.
Identifying the cause of childhood stroke may be straightforward or may require extensive clinical and neuroimaging expertise, serial evaluations, and reassessment based on the evolving clinical picture. ...
Identifying the cause of childhood stroke may be straightforward or may require extensive clinical and neuroimaging expertise, serial
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