Gotowe bibliografie tematyczne / Clumsiness in literature

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Gotowa bibliografia na temat „Clumsiness in literature”

Autor: Grafiati

Data publikacji: 26 lipca 2024

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Clumsiness in literature"

Ivry, Richard B. "Cerebellar Involvement in Clumsiness and Other Developmental Disorders." Neural Plasticity 10, no. 1-2 (2003): 141–53. http://dx.doi.org/10.1155/np.2003.141.

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Cerebellar abnormalities have been linked to a number of developmental disorders. Much evidence is based on the analysis of highresolution MRI scans. Imaging and behavioral studies have led researchers to consider functional contributions of the cerebellum beyond that associated with motor control. I review this literature, providing an analysis of different ways to consider the relation between cerebellar abnormalities and developmental disorders. Interestingly, although clumsiness is a problem of coordination, the contribution of cerebellar dysfunction to this developmental problem has recei

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Sannareddy, Rajesh, Rahul Lath, Michelle de Padua, and Alok Ranjan. "Meningioma with Intra- and Peritumoral Abscess." Indian Journal of Neurosurgery 07, no. 03 (2017): 220–22. http://dx.doi.org/10.1055/s-0037-1606820.

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AbstractThe association of meningioma with intra- and peritumoral brain abscess is rare. All cases reported in literature had some focus of infection in the body. We report a 56-year-old man with well-controlled diabetes mellitus found to have a space-occupying lesion upon evaluation for headache, vomiting, and clumsiness of right upper limb. Perioperatively, pus was found intra- and perilesionally around a thick, capsulated, dural-based, vascular lesion. Histopathology was suggestive of meningioma, and Escherichia coli was isolated upon culture.

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Reddy, Lankapothu Prem Balaji, Jagadeeshwar Kakumani, B. Srinidhi, and M. Sathish Kumar. "Sensory ganglionopathy and pituitary lesion in systemic lupus erythematosus: A case report and literature review." Romanian Journal of Rheumatology 34, no. 2 (2025): 85–90. https://doi.org/10.37897/rjr.2025.2.2.

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Background. Systemic lupus erythematosus (SLE) rarely manifests as sensory ganglionopathy or pituitary lesions, posing diagnostic challenges due to their atypical presentations and potential for irreversible damage. Case presentation. A 26-year-old male presented with five months of gait instability, numbness, and hand clumsiness, along with dry eyes and loose stools. Examination revealed sensory ataxia, absent reflexes, and positive anti-dsDNA antibodies, confirming SLE. Nerve conduction studies showed absent sensory nerve action potentials, consistent with sensory ganglionopathy. MRI identif

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Kresojevic, Nikola, Igor Petrovic, Natasa DragasevicMiskovic, and Vladimir Kostic. "Superficial siderosis: Case report and literature review." Srpski arhiv za celokupno lekarstvo 141, no. 3-4 (2013): 219–22. http://dx.doi.org/10.2298/sarh1304219k.

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Introduction. Superficial siderosis (SS) is caused by chronic subarachnoid bleeding and is characterized by free iron and hemosiderin deposition along the pial and subpial structures of central nervous system. SS leads to progressive and irreversible CNS damage. The most common causes of chronic subarachnoidal bleeding are tumors, head and spinal cord trauma, arteriovenous malformations and aneurysms. SS is characterized by clinical triad: sensorineural hearing loss, cerebellar ataxia and piramydal signs. Brain MR imaging is the investigation of choice for the diagnosis of SS. Typical findings

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Elvebakk, Kristine, Ingrid Elisabeth Johnsen, Cecilie Bendiksen Wold, Thomas Finsen, Harald Russwurm, and Vilhjalmur Finsen. "Simple Trapeziectomy for Arthrosis of the Basal Joint of the Thumb: 49 Thumbs Reviewed After Two Years." Hand Surgery 20, no. 03 (2015): 435–39. http://dx.doi.org/10.1142/s0218810415500367.

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Background: Many different surgical strategies for arthrosis of the carpometacarpal joint of the thumb are described in the literature. In 2010 we changed our routine procedure from an interposition arthroplasty using the abductor pollicis longus (APL) tendon to simple trapeziectomy without suspension or interposition. The purpose of this study was to review the clinical outcome after trapeziectomy and to compare it to those we had achieved with the APL procedure. Methods: We examined 49 hands operated with simple trapeziectomy during 2011-2012. Time between operation and review was 26 (15-26)

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Zaver, Dhillon B., and Nathan T. Douthit. "A Novel Mutation in the Adult-Onset Alexander’s Disease GFAP Gene." Case Reports in Medicine 2019 (January 10, 2019): 1–4. http://dx.doi.org/10.1155/2019/2986538.

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The case describes a 25-year-old Caucasian female diagnosed with Alexander’s disease (AxD) as an outpatient after extensive inpatient workup. Her presenting complaints included incontinence, clumsiness, seizures, dysphagia, and dysarthria. She was also found to have pancytopenia and dysautonomia. A full neurologic and hematologic workup yielded very little results, until a thorough literature search of her presenting complaints and radiologic findings pointed to adult-onset Alexander’s Disease. Alexander’s disease is a rare genetic leukodystrophy with a broad variety of presentations. Despite

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Mastrolilli, F., A. Benvenga, L. Di Biase, et al. "An Unusual Cause of Dementia: Essential Diagnostic Elements of Corticobasal Degeneration—A Case Report and Review of the Literature." International Journal of Alzheimer's Disease 2011 (2011): 1–6. http://dx.doi.org/10.4061/2011/536141.

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Corticobasal degeneration (CBD) is an uncommon, sporadic, neurodegenerative disorder of mid- to late-adult life. We describe a further example of the pathologic heterogeneity of this condition. A 71-year-old woman initially presented dysarthria, clumsiness, progressive asymmetric bradykinesia, and rigidity in left arm. Rigidity gradually involved ipsilateral leg; postural instability with falls, blepharospasm, and dysphagia subsequently developed. She has been previously diagnosed as unresponsive Parkinson's Disease. At our clinical examination, she presented left upper-arm-fixed-dystonia, spa

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Nardecchia, Francesca, Anna Caciotti, Teresa Giovanniello, et al. "3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature." International Journal of Molecular Sciences 23, no. 8 (2022): 4422. http://dx.doi.org/10.3390/ijms23084422.

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3-Methylglutaconic aciduria type I (MGCA1) is an inborn error of the leucine degradation pathway caused by pathogenic variants in the AUH gene, which encodes 3-methylglutaconyl-coenzyme A hydratase (MGH). To date, MGCA1 has been diagnosed in 19 subjects and has been associated with a variable clinical picture, ranging from no symptoms to severe encephalopathy with basal ganglia involvement. We report the case of a 31-month-old female child referred to our center after the detection of increased 3-hydroxyisovalerylcarnitine levels at newborn screening, which were associated with increased urina

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Sakaura, Hironobu, Yukihiko Yasui, Toshitada Miwa, Tomoya Yamashita, Kenji Ohzono, and Tetsuo Ohwada. "Cervical myelopathy caused by invagination of anomalous lamina of the axis." Journal of Neurosurgery: Spine 19, no. 6 (2013): 694–96. http://dx.doi.org/10.3171/2013.8.spine13325.

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The authors report a case of cervical myelopathy caused by invagination of the bilaterally separated lamina of the axis. They also present a literature review. The patient was a previously healthy 68-year-old man with a 1-year history of slowly progressive gait disturbance, right-hand clumsiness, and right dominant sensory disturbance in his trunk and extremities. Both MRI and CT showed that the spinal cord was markedly compressed at the C2–3 level, on the right side, by a deeply invaginated anomalous lamina of the axis. A bilaterally separated lamina was also visible. The patient underwent re

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Antonio Jesús, Morales Moreno, Castro Rey, Margarita del Carmen, et al. "A 19-Month-Old Spanish Boy with Anti-NMDAR Encephalitis: Case Report and Review of Literature." SVOA Neurology 5, no. 1 (2024): 21–25. http://dx.doi.org/10.58624/svoane.2024.05.0122.

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Background and Aim: The classic definition of acute encephalitis consists of altered consciousness associated with fever, seizures or focal neurological alterations on neuroimaging or electroencephalography. However, there are particularities that may provide a glimpse of the probably autoimmune versus infectious etiology of the same neurological picture. Case presentation: A 19-month-old male starts with motor clumsiness and refusal to ambulation and leg claudication in the context of febrile pharyngotonsillitis. Simultaneously, first episode of forced gaze’s lateralization and cephalic devia

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Książki na temat "Clumsiness in literature"

Henning, Adeline. Je suis adroit, je suis maladroit. Haiter, 2000.

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Carle, Eric. The very clumsy click beetle. Hamish Hamilton, 1999.

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Carle, Eric. The very clumsy click beetle. Philomel Books, 1999.

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Carle, Eric. The very clumsy click beetle. Philomel Books, 1999.

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Roger, Hargreaves. Mr. Bump. 4th ed. PSS! Price Stern Sloan, 2011.

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Roger, Hargreaves. Mr Bump. Thurman, 1986.

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Roger, Hargreaves. Mr. Bump: A pop-up adventure. World International Pub., 1993.

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Ungeschickt: Eine Fallgeschichte der deutschen Literatur. Brill, Wilhelm Fink, 2021.

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Carle, Eric. The Very Clumsy Click Beetle's Favorite Words (The World of Eric Carle). Grosset & Dunlap, 2008.

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Carle, Eric. KLICK musst du machen, kleiner Käfer. Gerstenberg, 2000.

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Części książek na temat "Clumsiness in literature"

Patterson, Jonathan. "‘Greatness going off’ in Renaissance Antony and Cleopatra Tragedies." In Literature, Learning, and Social Hierarchy in Early Modern Europe. British Academy, 2022. http://dx.doi.org/10.5871/bacad/9780197267332.003.0010.

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The suicides of Antony and Cleopatra afforded the Renaissance dramatist various angles on what Shakespeare called ‘Greatness going off’. Renaissance Antony and Cleopatra tragedies in France and England pointedly thematised how the great failed to preserve the dignity of their rank and office in life, and how they fell short of securing personal posthumous renown in death. Antony and his Egyptian queen found themselves unexpectedly upstaged by social inferiors. Renaissance tragedians noted the irony of Antony’s incompetent imitation of his slave, Eros, who took his own life rather than his mast

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