Zaloguj się

Gotowe bibliografie tematyczne / Chorioretinal lacunae / Artykuły w czasopismach

Kliknij ten link, aby zobaczyć inne rodzaje publikacji na ten temat: Chorioretinal lacunae.

Artykuły w czasopismach na temat „Chorioretinal lacunae”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Sprawdź 26 najlepszych artykułów w czasopismach naukowych na temat „Chorioretinal lacunae”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.

1

Sinha, Ayushi, and Anamika Nath. "Chorioretinal lacunae." Indian Journal of Ophthalmology - Case Reports 3, no. 2 (2023): 636. http://dx.doi.org/10.4103/ijo.ijo_165_23.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

2

Tripathy, Koushik, Rohan Chawla, and Divya Betala. "Seizures and chorioretinal lacunae in an infant." Journal of Paediatrics and Child Health 53, no. 9 (2017): 919. http://dx.doi.org/10.1111/jpc.1_13465.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

3

ITURRALDE, DIANA, CATHERINE B. MEYERLE, and LAWRENCE A. YANNUZZI. "Aicardi Syndrome: Chorioretinal Lacunae Without Corpus Callosum Agenesis." Retina 26, no. 8 (2006): 977–78. http://dx.doi.org/10.1097/01.iae.0000224937.78389.15.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

4

International, Journal of Medical Science and Innovative Research (IJMSIR). "A case report on Aicardi Syndrome." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 4 (2024): 03–08. https://doi.org/10.5281/zenodo.15422265.

Pełny tekst źródła

Streszczenie:

<strong>Abstract</strong> Aicardi syndrome is a genetic disorder linked to the X chromosome, predominantly affecting females. Diagnosis requires the presence of three key features: absence of the corpus callosum, infantile spasms, and chorioretinal lacunae. This case study details the presentation of a female newborn delivered at 36weeks gestation, who presented to the emergency department with arm and leg stiffness. An electroencephalogram confirmed generalized hypsarrhythmia, characteristic of infantile spasms. Magnetic resonance imaging revealed complete absence of the corpus callosum. Subs

Style APA, Harvard, Vancouver, ISO itp.

5

de Leeuw, Carola, Anne Kurver, and Aad Verrips. "Chorioretinal Lacunae in Aicardi's Syndrome: Key for the Diagnosis." Neuropediatrics 51, no. 04 (2020): 311–12. http://dx.doi.org/10.1055/s-0040-1709454.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

6

Bayram-Suverza, Mauricio, Karla Alejandra Torres-Navarro, Ángeles Yahel Hernández-Vázquez, and Juan Abel Ramírez-Estudillo. "Microcephaly and Chorioretinopathy Relevance as a Differential Diagnosis." Diagnostics 13, no. 15 (2023): 2588. http://dx.doi.org/10.3390/diagnostics13152588.

Pełny tekst źródła

Streszczenie:

Microcephaly and chorioretinopathy are genetic disorders that are inherited in an autosomal recessive manner. The most frequent ocular manifestation is the presence of lacunar atrophy in the retina and choroid. The diagnosis of this condition can be challenging as several potential causes and related syndromes need to be ruled out. We present two cases of microcephaly and chorioretinopathy in Mexican patients, their clinical characterization, and discuss the differential diagnoses that should be considered. An 8-year-old girl was examined due to a history of decreased vision in both eyes. Fund

Style APA, Harvard, Vancouver, ISO itp.

7

Aicardi, Jean. "Callosal agenesis, chorioretinal lacunae, absence of infantile spasms, and normal development: Aicardi syndrome without epilepsy?" Developmental Medicine & Child Neurology 47, no. 6 (2007): 364. http://dx.doi.org/10.1111/j.1469-8749.2005.tb01153.x.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

8

Viñas, Jose Maria Prats, María Jesús Martinez Gonzalez, Ainhoa Garcia Ribes, Sonia Martinez Gonzalez, and Ricardo Martinez Fernandez. "Callosal agenesis, chorioretinal lacunae, absence of infantile spasms, and normal development: Aicardi syndrome without epilepsy?" Developmental Medicine & Child Neurology 47, no. 6 (2007): 419–20. http://dx.doi.org/10.1111/j.1469-8749.2005.tb01164.x.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

9

Viñas, Jose Maria Prats, María Jesús Martinez Gonzalez, Ainhoa Garcia Ribes, Sonia Martinez Gonzalez, and Ricardo Martinez Fernandez. "Callosal agenesis, chorioretinal lacunae, absence of infantile spasms, and normal development: Aicardi syndrome without epilepsy?" Developmental Medicine & Child Neurology 47, no. 6 (2005): 419–20. http://dx.doi.org/10.1017/s0012162205000812.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

10

Aicardi, Jean. "Callosal agenesis, chorioretinal lacunae, absence of infantile spasms, and normal development: Aicardi syndrome without epilepsy?" Developmental Medicine & Child Neurology 47, no. 6 (2005): 364. http://dx.doi.org/10.1017/s001216220521071x.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

11

Aguiar, Maria de Fátima M., Marisa Cavalcanti, Hamilton Barbosa, Suzete Leme Vilela, José Luiz Mendonça, and Elaine Horta. "Síndrome de Aicardi e papiloma do plexo coróide: uma associação rara. Relato de caso." Arquivos de Neuro-Psiquiatria 54, no. 2 (1996): 313–17. http://dx.doi.org/10.1590/s0004-282x1996000200022.

Pełny tekst źródła

Streszczenie:

Relata-se o caso clínico de uma criança de 5 meses de idade, do sexo feminino, com achados característicos da síndrome de Aicardi: agenesia do corpo caloso, espasmos infantis, anormalidades oculares ("chorioretinal lacunae" e microftalmia), atraso do desenvolvimento neuropsicomotor e malformações vertebrais com cifoescoliose. Os exames complementares confirmaram o diagnóstico e as imagens neurorradiológicas evidenciaram, além da agenesia do corpo caloso, massa localizada em região atrioventricular esquerda (papiloma do plexo coróide). A síndrome de Aicardi associada a papiloma do plexo coróide

Style APA, Harvard, Vancouver, ISO itp.

12

Broomall, Eileen, Deborah Renaud, Rafif Ghadban, Ralitza Gavrilova, and Michael C. Brodsky. "Peripapillary Chorioretinal Lacunae in a Girl With 3q21.3 to 3q22.1 Microdeletion With Features of Aicardi Syndrome." JAMA Ophthalmology 131, no. 11 (2013): 1485. http://dx.doi.org/10.1001/jamaophthalmol.2013.4830.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

13

Ha, Thuong T., Rosemary Burgess, Morgan Newman, et al. "Aicardi Syndrome Is a Genetically Heterogeneous Disorder." Genes 14, no. 8 (2023): 1565. http://dx.doi.org/10.3390/genes14081565.

Pełny tekst źródła

Streszczenie:

Aicardi Syndrome (AIC) is a rare neurodevelopmental disorder recognized by the classical triad of agenesis of the corpus callosum, chorioretinal lacunae and infantile epileptic spasms syndrome. The diagnostic criteria of AIC were revised in 2005 to include additional phenotypes that are frequently observed in this patient group. AIC has been traditionally considered as X-linked and male lethal because it almost exclusively affects females. Despite numerous genetic and genomic investigations on AIC, a unifying X-linked cause has not been identified. Here, we performed exome and genome sequencin

Style APA, Harvard, Vancouver, ISO itp.

14

Rao, T. Rama, Dwip Jyoti Kalita, and Shahzad Alam. "Aicardi Syndrome: Case Series." International Journal of Health Sciences and Research 14, no. 10 (2024): 176–81. http://dx.doi.org/10.52403/ijhsr.20241018.

Pełny tekst źródła

Streszczenie:

Aicardi syndrome is a rare genetic disorder that primarily affects females and is marked by three main clinical features: agenesis of the corpus callosum, chorioretinal lacunae, and seizures. The absence or abnormal development of the corpus callosum impairs communication between the brain's hemispheres, resulting in various neurological issues. Seizures, commonly appearing as infantile spasms, are frequent and can vary in severity and frequency. Aicardi syndrome is usually diagnosed in infancy through clinical evaluation and imaging studies. Effective care and management of Aicardi syndrome r

Style APA, Harvard, Vancouver, ISO itp.

15

Sözüöz, Melis Arda, Ezgi Aydın Varol, and Merve Aksoy. "Pediatric dentistry approach in a child with Aicardi-Goutières Syndrome type 2: A case report and literature review." Contemporary Pediatric Dentistry 5, no. 2 (2024): 105–12. http://dx.doi.org/10.51463/cpd.2024.20.

Pełny tekst źródła

Streszczenie:

Aicardi-Goutières Syndrome is a rare autosomal recessive disorder characterized by a triad of partial or complete agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae. The condition predominantly affects females, as males often do not survive the embryonic period. Intellectual disability associated with the syndrome ranges from mild to moderate. There is limited information in the literature regarding the oral manifestations of this syndrome. This case report aims to provide insights into the development of primary dentition in patients with Aicardi-Goutières Syndrome a

Style APA, Harvard, Vancouver, ISO itp.

16

Hashemi, Kattayoon, Elias I. Traboulsi, Richard Chavis, Nina Scribanu, and Georgia A. Chrousos. "Chorioretinal Lacuna in the Amniotic Band Syndrome." Journal of Pediatric Ophthalmology & Strabismus 28, no. 4 (1991): 238–39. http://dx.doi.org/10.3928/0191-3913-19910701-12.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

17

Constad, William H., Rudolph S. Wagner, and Anthony R. Caputo. "Aicardi Syndrome in One Dizygotic Twin." Pediatrics 76, no. 3 (1985): 450–53. http://dx.doi.org/10.1542/peds.76.3.450.

Pełny tekst źródła

Streszczenie:

The Aicardi syndrome consists of infantile spasms, defects of the corpus callosum, dorsal vertebral anomalies, and chorioretinal lacunar defects. The etiology is, as yet, unknown. The most likely cause, however, is an χ-linked mutational event that is lethal in males. The first case of the Aicardi syndrome known to occur in one twin is reported. The patient was female and her unaffected sibling was male. This provides strong evidence to support the theory of an χ-linked mutational event as the cause of this condition. The typical chorioretinal defects, often difficult to document because these

Style APA, Harvard, Vancouver, ISO itp.

18

Guerriero, Silvana, Vittorio Sciruicchio, Roberto De Blasi, et al. "Chorioretinal Lacunae: Pathognomonic Findings for Aicardi Syndrome." Journal of Pediatric Ophthalmology & Strabismus, August 10, 2009. http://dx.doi.org/10.3928/01913913-20090701-04.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

19

Guerriero, Silvana, Vittorio Sciruicchio, Roberto De Blasi, et al. "Chorioretinal Lacunae: Pathognomonic Findings for Aicardi Syndrome." Journal of Pediatric Ophthalmology & Strabismus, May 21, 2010. http://dx.doi.org/10.3928/01913913-20100324-03.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

20

"Seizures and chorioretinal lacunae in an infant." Journal of Paediatrics and Child Health 53, no. 9 (2017): 920. http://dx.doi.org/10.1111/jpc.2_13465.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

21

Al-Moujahed, Ahmad, Natalia F. Callaway, Cassie A. Ludwig, Nadim Rayess, Edward Wood, and Darius M. Moshfeghi. "Morning glory optic nerve in Aicardi syndrome: Report of a case with fluorescein angiography." European Journal of Ophthalmology, July 16, 2020, 112067212094270. http://dx.doi.org/10.1177/1120672120942702.

Pełny tekst źródła

Streszczenie:

Background: Aicardi syndrome is an X-linked condition that is associated with multiple ophthalmic malformations. Here, we report the first published fluorescein angiography (FA) study of a morning glory optic nerve in a patient with Aicardi syndrome and contralateral persistent fetal vasculature (PFV). Case description: A 12-day old full-term baby girl with a normal neurological exam was referred for evaluation of microphthalmia. The posterior segment of the right eye demonstrated chorioretinal lacunae typical of Aicardi syndrome and microphthalmos with a stalk consistent with PFV. The right e

Style APA, Harvard, Vancouver, ISO itp.

22

Shaikh, Nawazish, Bharat Arora, and Vinod Kumar. "KIF11 Mutation with Congenital Microcephaly and Chorioretinal Lacunae." Ophthalmology Retina, July 2022. http://dx.doi.org/10.1016/j.oret.2022.06.002.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

23

Dias, Edwin. "Aicardi Syndrome in a 8 month Old Female Child." International Journal of Health Sciences and Pharmacy, April 19, 2019, 18–20. http://dx.doi.org/10.47992/ijhsp.2581.6411.0039.

Pełny tekst źródła

Streszczenie:

Aicardi syndrome (AS) is a triad of infantile spasms, chorioretinal ‘lacunae’ and agenesis of corpus callosum. The exact frequency of this condition is not known. Here we provide a description of an 8 month old child with Aircardi syndrome. Treated with multiple Antiepileptic drug.

Style APA, Harvard, Vancouver, ISO itp.

24

Edwin, Dias, and Sara Mathew Chris. "Respiratory Therapy Interventions preventing the Need for Bronchoscopy in a 12 year old, with Right Lower lobe Atelectasis -A Case Report." International Journal of Health Science and Pharmacy 3, no. 1 (2019). https://doi.org/10.5281/zenodo.2646469.

Pełny tekst źródła

Streszczenie:

Aicardi syndrome (AS) is a triad of infantile spasms, chorioretinal ‘lacunae’ and agenesis of corpus callosum. The exact frequency of this condition is not known. Here we provide a description  of an 8 month old child with Aircardi syndrome. Treated with multiple Anti- epileptic drugs.  

Style APA, Harvard, Vancouver, ISO itp.

25

Pathak, Pradnya Dileep, Preetam P. Shah, Laxmi S. Lakade, and Maya U. Shinde. "Full Mouth Rehabilitation of a Child with Aicardia-Goutières: A Rare Syndrome." JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2023. http://dx.doi.org/10.7860/jcdr/2023/58913.17383.

Pełny tekst źródła

Streszczenie:

Aicardi-Goutières Syndrome (AGS) is a rare genetic disorder with autosomal recessive inheritance. AGS is characterised by an earlyonset encephalopathy that usually, but not always, results in severe intellectual and physical disability. Involuntary muscular spasms between the ages of four months and four years are the typical starting point for Aicardi syndrome. Hepatosplenomegaly, increased liver enzymes, thrombocytopenia, and abnormal neurologic signs in a subgroup of AGS children at birth strongly imply congenital infection. Agenesis of the corpus callosum, chorioretinal lacunae, and seizur

Style APA, Harvard, Vancouver, ISO itp.

26

Masnada, Silvia, Anna Pichiecchio, Manuela Formica, et al. "Basal ganglia dysmorphism in patients with Aicardi syndrome." Neurology, December 4, 2020, 10.1212/WNL.0000000000011237. http://dx.doi.org/10.1212/wnl.0000000000011237.

Pełny tekst źródła

Streszczenie:

ObjectiveAiming to detect associations between neuroradiologic and EEG evaluations and long-term clinical outcome in order to detect possible prognostic factors, a detailed clinical and neuroimaging characterization of 67 cases of Aicardi syndrome (AIC), collected through a multicenter collaboration, was performed.MethodsOnly patients who satisfied Sutton diagnostic criteria were included. Clinical outcome was assessed using gross motor function, manual ability, and eating and drinking ability classification systems. Brain imaging studies and statistical analysis were reviewed.ResultsPatients

Style APA, Harvard, Vancouver, ISO itp.

Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!