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Gotowe bibliografie tematyczne / Partial Atrophic Tongue

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Artykuły w czasopismach

Gotowa bibliografia na temat „Partial Atrophic Tongue”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Partial Atrophic Tongue"

1

Terai, H., and M. Shimahara. "Partial atrophic tongue other than median rhomboid glossitis." Clinical and Experimental Dermatology 32, no. 4 (2007): 381–84. http://dx.doi.org/10.1111/j.1365-2230.2007.02383.x.

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Skakodub, A. A., N. А. Geppe, O. I. Admakin, et al. "Clinical and X-ray diagnostic criteria for maxillofacial damage in children with juvenile limited scleroderma." Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 65, no. 2 (2020): 71–79. http://dx.doi.org/10.21508/1027-4065-2020-65-2-71-79.

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The objective of our study was to improve the diagnosis of maxillofacial lesions in children with juvenile scleroderma. We performed a dental examination of 41 children from 4 to 17 years old with juvenile scleroderma. Based on the clinical X-ray examination we identified the main diagnostic signs of the maxillofacial damage in children with juvenile scleroderma, including partial hemiatrophy, plaque or linear facial lesions, reduced salivation, atrophic glossitis, plaque spots of mucous tongue atrophy, ischemia or shortening of the sublingual bridle, local recession of the gums of the lower j

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3

Petruzzi, M., M. De Benedittis, L. Pasture, G. Pannone, F. R. Grassi, and R. Serpico. "Isolated Lichen Planus of the Lip." International Journal of Immunopathology and Pharmacology 20, no. 3 (2007): 631–35. http://dx.doi.org/10.1177/039463200702000321.

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Oral lichen planus (OLP) is a relatively common disorder whose cause is still unknown. It occurs mostly on the buccal mucosa, but the gingivae, tongue, floor of the mouth and retromalar pads may also be affected. It rarely occurs on the lips and usually in association with oral lesions. We report a case series of ten patients with a history of isolated swelling of the lower and/or upper lip, erosions and crusting. General medical history, examination of the oral cavity and recording of signs and symptoms were carried out for each patient. Among the six different clinical variants of OLP descri

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4

Chambers, Kyle J., Douglas C. Anthony, Gregory W. Randolph, Christopher J. Hartnick, Edward G. Stopa, and Phillip C. Song. "Atrophy of the tongue following complete versus partial hypoglossal nerve transection in a canine model." Laryngoscope 126, no. 12 (2016): 2689–93. http://dx.doi.org/10.1002/lary.26065.

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Shurygin, Konstantin N., Roman S. Matveev, and Bulat N. Khanbikov. "PROBLEMS OF ADAPTATION TO REMOVABLE PROSTHESES IN PATIENTS OF DIFFERENT AGE GROUPS." Acta medica Eurasica, no. 2 (June 26, 2023): 53–59. http://dx.doi.org/10.47026/2413-4864-2023-2-53-59.

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Adentia is a fairly wide-spread condition among the population. Even at current level of dentistry and materials science development the proportion of patients who do not use removable prostheses, according to various data from foreign and domestic researchers, reaches almost a third. Due to the fact that removable prostheses are combined irritants of prosthetic bed tissues, adaptation to them is an urgent problem of orthopedic dentistry. The process of adaptation to prostheses, according to Russian researchers, takes place on average in the period of 10 to 33 days and depends on many factors,

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6

Dos Santos, Marilúcia Campos, Zânder Fernandes Teixeira De Azevedo, Ariana Lima Pereira, et al. "Dicephalia in a Bovine." Acta Scientiae Veterinariae 44, no. 1 (2016): 3. http://dx.doi.org/10.22456/1679-9216.84120.

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Background: Congenital defects consist of structural or functional abnormalities present at birth, which partially or globally affect the systems. Among the defects are the conjoined twins, a rare congenital anomaly caused by fusion of two monozygotic embryos which can be classified according to the different sites of union. The Siamese twins and embryonic duplication are represented by a progressive series of malformations, since partial duplication of part of the body to the training almost full two bodies. Siamese twins occur in humans and in several animal species. Dicephalia refers to two

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7

Terai, H., N. Fukui, S. Kasuya, N. Hashiguchi, and T. Ueno. "Clinical Features of Partial Atrophic Tongue Associated with Candida." January 5, 2016. https://doi.org/10.19070/2377-8075-1600037.

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Background: Clinical features of partial atrophic tongue associated with Candidia including median rhomboid glossitis have not been established. Methods: We enrolled 90 patients with atrophic tongue who were referred to our department with the chief symptom of tongue pain when eating spicy or hot food. They were diagnosed as having oral candidiasis, and were successfully treated with anti-fungal agents. The patients were divided into groups, based on partial atrophic (n = 29) or total atrophic tongue (n = 61). Age at presentation, sex, duration of tongue pain, other signs and symptoms, complet

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8

H, Terai, Fukui N, Kasuya S, Hashiguchi N, and Ueno T. "Clinical Features of Partial Atrophic Tongue Associated with Candida." International Journal of Dentistry and Oral Science, January 5, 2016, 177–80. http://dx.doi.org/10.19070/2377-8075-1600037.

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9

Chen, Guan-Ying, Zhi-Qun Tang, and Zhe-Xuan Bao. "Vitamin B12 deficiency may play an etiological role in atrophic glossitis and its grading: A clinical case-control study." BMC Oral Health 22, no. 1 (2022). http://dx.doi.org/10.1186/s12903-022-02464-z.

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Abstract Background Existing studies have reported the significant association between atrophic glossitis (AG) and hematinic deficiencies, including iron, folate and vitamin B12 deficiency. However, these findings were inconsistent. AG can be graded as partial or complete atrophy. It is still unclear whether hematinic deficiencies are associated with the grading of AG. Methods 236 AG patients and 208 sex- and age-matched healthy controls were enrolled in this study. Hematological tests including complete blood count, and serum levels of folate, ferritin and vitamin B12 were performed. The AG g

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10

Mishra, Shamli, and Manoj Kumar Mohapatra. "A RARE CASE OF MADRAS VARIANT OF MOTOR NEURON DISEASE." INDIAN JOURNAL OF APPLIED RESEARCH, April 1, 2023, 8. http://dx.doi.org/10.36106/ijar/9608842.

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INTRODUCTION: Madras variant MND is a rare entity is characterized by multiple lower cranial nerve palsies(7-12) and atrophy of limbs. A 26 year old male presented with complaints of difculty i BACKGROUND: n hearing and hoarseness of voice since 1 year and weakness of lower limbs since 10 days without any sensory, bowel and bladder symptoms. On examination, his vitals were stable. Cranial nerves examination revealed abnormality in the form of b/l sensorineural hearing loss, weakness of b/l facial muscles with fasiculations, absent gag reex with atrophy and fasiculations of the tongue. There

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