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Gotowe bibliografie tematyczne / Semi-lobar

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Gotowa bibliografia na temat „Semi-lobar”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Semi-lobar"

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Taori, K., N. Sardesai, V. Ingle, and V. Patil. ""Semi lobar holoprosencephaly"- a case report." Indian Journal of Radiology and Imaging 15, no. 4 (2005): 576. http://dx.doi.org/10.4103/0971-3026.29177.

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Kandoussi, Hajar, Khaoula Laaboub, Hounaida Mahfoud, and Zaki Elhanchi. "Semi-Lobar Holoprosencephaly Diagnosed at Term: The Critical Role of Prenatal Diagnosis." Scholars Journal of Medical Case Reports 13, no. 07 (2025): 1574–77. https://doi.org/10.36347/sjmcr.2025.v13i07.012.

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Objective: To report a case of semi-lobar holoprosencephaly (HPE) diagnosed at term in the context of an unmonitored diabetic pregnancy, emphasizing the importance of early prenatal screening. Case Report: A primigravida with poorly controlled type 1 diabetes and no structured prenatal care was admitted in preterm labor at 36 weeks. An emergency ultrasound revealed intrauterine growth restriction, microcephaly, and semi-lobar HPE with major facial dysmorphism (hypotelorism, single nostril). The infant was delivered vaginally. At birth, the newborn exhibited profound clinical signs of life-thre

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Jing, Hongkui, Judy Flax, Cynthia P. Roesler, Naseem Choudhury, and April A. Benasich. "Auditory event-related responses in children with semi-lobar holoprosencephaly." Brain and Development 28, no. 4 (2006): 207–14. http://dx.doi.org/10.1016/j.braindev.2005.07.005.

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Jalal, Mohammed, Imane El Abbassi, Ayoub Amghar, Amine Lamrissi, and Said Bouhya. "Alobar holoprosencephaly: A case report." Edorium Journal of Gynecology and Obstetrics 7, no. 2 (2023): 1–4. http://dx.doi.org/10.5348/100032g06mj2023cr.

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Introduction: Holoprosencephaly (HPE) is a rare brain malformation, which results from a cleavage defect of the prosencephalon. Three forms have been described as: alobar, semi-lobar, and lobar forms. Case Report: We report a rare case of holoprosencephaly, diagnosed at the maternity of the Ibn Rochd Hospital Center in Casablanca. Conclusion: Holoprosencephaly is secondary to a cleavage anomaly of the prosencephalon, the diagnosis is based on echotomography, computed tomography (CT) scan and nuclear magnetic resonance imaging (MRI). It is important to perform a karyotype to look for a chromoso

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International, Journal of Medical Science and Innovative Research (IJMSIR). "Holoprosencephaly – Case Reports of A Rare Neurological Malformation." 2458-8687 9, no. 6 (2024): 07–12. https://doi.org/10.5281/zenodo.15448661.

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<strong>Abstract</strong> Holoprosencephaly (HPE) is a complex structural anomaly of the developing forebrain caused by incomplete division of prosencephalon into two separate hemispheres and ventricles resulting in dysmorphism of brain and face and neurological impairment. HPE has incidence rate of 1:250 in utero and the live birth rate is 1:16,000. It is classified into three types based on the degree of cerebral involvement; lobar, semi-lobar and alobar. There are various etiological factors involved in causation of Holoprosencephaly including environmental, chromosomal and genetic syndrome

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Sharif, Md Mofazzal, Khaleda Parvin, Md Towhidur Rahman, Nayeem Ullah, and Saiful Islam. "Two Cases of Holoprosencephalies." KYAMC Journal 8, no. 1 (2017): 64–68. http://dx.doi.org/10.3329/kyamcj.v8i1.33878.

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Two pregnant women with around 33-34 weeks of gestation were reported to Gynaecology and Obstetrics OPD of North Bengal Medical College Hospital, Bangladesh for last trimester antenatal checkup. They were primigravida with around 23-25 years of ages without previous antenatal check up. Both of them had normal course of pregnancy. Ultrasounds of pregnancy profile were done. It was observed in first case that septum pellucidum was absent in brain with partially formed falx cerebri, interhemispheric fissure. Occipital horn was rudimentary and thalami and basal ganglia were partially separated. Th

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Razali, Renardy Reza, and Muhammad Ilham Harahap. "Cyclopia syndrome in a 34-week foetus." International Surgery Journal 11, no. 7 (2024): 1165–67. http://dx.doi.org/10.18203/2349-2902.isj20241748.

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Cyclopia is a rare genetic birth defect with an incidence of approximately 1 in 13,000 to 20,000 newborns. This condition is marked by the failure of the eye orbits to properly divide, resulting in a single eye field or closely positioned eye fields. Additional features include a missing or dysfunctional nose and malformed ears. Most embryos with this condition are aborted, stillborn, or die shortly after birth. This case report discusses the 34-week pregnancy of a 36-year-old woman referred to Arifin Achmad Hospital. Ultrasound revealed midline fusion of the foetal head and thalamus, leading

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Novosadova, O. A., V. N. Grigoryeva, P. A. Astanin, M. A. Lesnikov, and A. S. Samodurov. "Clinical and non-hemorrhagic neuroimaging indicators of probable cerebral amyloid angiopathy as a cause of non-traumatic lobar hematomas." Perm Medical Journal 41, no. 3 (2024): 15–27. http://dx.doi.org/10.17816/pmj41315-27.

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Objective. To identify clinical and non-hemorrhagic neuroimaging indicators of probable CAA in patients with acute non-traumatic lobar hematomas. Cerebral amyloid angiopathy (CAA) is a microangiopathy affecting the leptomeningial and cortical vessels of the brain due to the deposition of pathological b-amyloid in them. The most common clinical manifestation of CAA is lobar hematomas (LH) – spontaneous intracerebral hemorrhages localized between the cerebral cortex and basal ganglia. LH can also occur in hypertensive cerebral microangiopathy (hCMA) in patients with arterial hypertension. Since

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Shrestha, Dhruba, Ganendra Raya, Amar Prajapati, Suruchi Dhaubhadel, Sushmita Puri, and Dybesh Regmi. "Radiographically Confirmed Community-Acquired Pneumonia in Pediatric Patients Prior to Pneumococcal Vaccination in Nepal." Journal of Pediatric Infectious Diseases 13, no. 01 (2017): 057–62. http://dx.doi.org/10.1055/s-0037-1607266.

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Background The massive burden of pediatric pneumonia is associated with high morbidity and mortality, particularly in developing countries where immunization programs are absent or recently been implemented. The objective of this study was to describe the number of hospitalizations and outcomes of children aged 1 month to 10 years with community-acquired pneumonia (CAP) between January 1, 2014, and June 30, 2015, in semi-rural Nepal. Methods This retrospective study was undertaken prior to the implementation of the pneumococcal conjugate vaccination (PCV) program in Bhaktapur district of Nepal

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Jahan Khan, M. Delwar, M. Ashraful Islam, Kazi Raiyan Hoque, et al. "The relationship between lobar distribution and primary lung cancer histological types." International Journal of Advances in Medicine 11, no. 5 (2024): 449–54. http://dx.doi.org/10.18203/2349-3933.ijam20242307.

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Background: Lung cancer is the primary cause of cancer-related deaths globally. Accurate tumor location and subtype characterization are critical for optimizing treatment and predicting outcomes. This study aims to identify the relationship between lobar distribution and primary lung cancer histological types and describe the most recent patterns at the country-level origin. Methods: This cross-sectional study was conducted at a major tertiary care hospital in Bangladesh, including 165 patients recruited using purposive non-probability sampling. Data were collected using a semi-structured case

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Streszczenia konferencji na temat "Semi-lobar"

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Zhang, Guodong, Xin Zhang, Hong Zhao, and Peiyu Yan. "A Semi-automatic Extraction Algorithm of Lung Lobar Fissures from HRCT Images Using Ridgelet." In 2008 International Conference on Biomedical Engineering And Informatics (BMEI). IEEE, 2008. http://dx.doi.org/10.1109/bmei.2008.94.

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