7 results on '"Nguyen Thanh Van"'
Search Results
2. Research on Macroanatomic and Histologic Characteristics of the Lower Lateral Nasal Cartilages in Vietnamese
- Author
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Pham Dang Dieu, Vu Thi Nga, Nguyen Thanh Van, Nguyen Duy Bac, Toi Chu Dinh, Ho Nguyen Anh Tuan, Nguyen Thi Thu Phuong, and Tran Dang Khoa
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3.0 tesla scanner ,business.industry ,lcsh:R ,Diffusion tensor tractography ,lcsh:Medicine ,General Medicine ,Anatomy ,Human brain ,Nasal tip ,Fat pad ,Dome (geology) ,Lower lateral cartilages ,Lateral cartilage ,Cadaver ,interdomal ligament ,Lobular segment ,Medicine ,Somatosensory thalamocortical tract ,Nasal cartilages ,interdomal fat pad ,business ,Basic and Clinical Medical Researches in Vietnam - Abstract
BACKGROUND: There are recently many studies about the anatomy of lower lateral cartilage (LLC). However, the microanatomic studies to identify the segments of most LLC at the nasal tip in Vietnamese are very rare. AIM: Investigate the macroanatomic and microanatomic characteristics of the LLC and the structures of the nasal tip. METHODS: Descriptive study, 30 cadaver noses fixed by 10% formalin, 2 cadaver noses fixed by HE in 69 Institutes in Vietnam from December 2017 to April 2019. RESULTS: The average length of the medial crus is 12.3 mm on the right and 13.2 mm on the left. The maximum intercrural distance is 10.7 mm. The average length of the dome is 3.7 mm and 3.9 mm on the right and left side separately, with 2 subunits are the domal and lobular segment. The average thickness of the tip points is 1.0 mm. The width of the interdomal and intercrural ligaments are 0.5-fold the height and 2-fold the thickness. The thickness of the interdomal fat pad is 3mm and about 0.5-fold the wide. CONCLUSION: The LLC has 3 parts: intermediate, medial and lateral crus. The microanatomic structures of tip consist of the interdomal ligaments, intercrural ligaments, SMAS and interdomal fat pad.
- Published
- 2019
3. The Correlation between the Structures of the Nasal Tip on the Ultrasound and the Anthropometry of the Nose in Vietnamese
- Author
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Tran Dang Khoa, Nguyen Thanh Van, Ho Nguyen Anh Tuan, Nguyen Duy Bac, Pham Dang Dieu, Nguyen Thi Phuong, Vu Thi Nga, and Toi Chu Dinh
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business.industry ,Ultrasound ,lcsh:R ,lcsh:Medicine ,General Medicine ,Anatomy ,Anthropometry ,Nasal tip ,Fat pad ,The nasal tip ,medicine.anatomical_structure ,Tip point ,The interdomal fat pad ,The protrusion of the nasal tip ,Medicine ,business ,Nose ,Basic and Clinical Medical Researches in Vietnam - Abstract
BACKGROUND: Nowadays, there are few types of research held in Vietnam to investigate the anthropometric index of the nose as well as analysis the structure of nasal tip on ultrasound to identify the relationship between these parameters. AIM: determine the relationship between the height and the width of the nasal tip and the structures constructed these areas by anthropometric and ultrasound measurement. METHODS: a descriptive study in Thanh Van Hospital from December 2017 to April 2019. RESULTS: There were 94 women (62.7%), and 56 men (37.3%) and the average age were 33.6 years old. The height and width of the nasal tip are 10.1 mm and 21.7 mm, respectively. Through the ultrasound, the thickness of the adipose tissues is 3 mm. The width of the interdomal fat pad is 6.5 mm and the distance between two tip point is 5.6 mm. There are the relationships between the distance of two tip points and the width of the tip (r = 0.341), and the width of the interdomal fat pad (r = 0.72). There is also the correlation between the width of the nasal tip with the distance of two tip points (r = 0.46) and the height of the tip with the thickness of the interdomal fat pad (r = 1.23). CONCLUSION: The thickness of the interdomal fat affects the height of the tip, and the distance of two tip points influences the width of the tip.
- Published
- 2019
4. McCune-Albright syndrome onset with vaginal bleeding
- Author
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Vuong Kim Ngan, Nguyen Thanh Van Anh, Nguyen Minh Duc, and Ngo Van Doan
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medicine.medical_specialty ,media_common.quotation_subject ,Puberty, Precocious ,030209 endocrinology & metabolism ,Physical examination ,Fibrous Dysplasia, Polyostotic ,McCune–Albright syndrome ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Humans ,Medicine ,Precocious puberty ,Vaginal bleeding ,Girl ,Polyostotic fibrous dysplasia ,media_common ,medicine.diagnostic_test ,business.industry ,Cafe-au-Lait Spots ,Genetic disorder ,General Medicine ,medicine.disease ,Dermatology ,Child, Preschool ,Skin hyperpigmentation ,Female ,Uterine Hemorrhage ,medicine.symptom ,business - Abstract
McCune-Albright syndrome (MAS), a rare genetic disorder, affects multiple organs and classically presents with the triad of polyostotic fibrous dysplasia (FD), skin hyperpigmentation (café-au-lait spots) and precocious puberty. Diagnosis occurs when patients manifest at least two of these three symptoms. We describe a 4-year-old girl who was admitted to our hospital due to recurrent vaginal bleeding, initially diagnosed as precocious puberty. On brain MRI, abnormalities in the maxillary and occipital bones were compatible with FD. Clinical examination after craniofacial bone lesions and clinical signs indicated MAS revealed abnormally pigmented macules on the neck and back, which were initially overlooked. No abnormal hormone tests were observed. Precocious puberty is the most common MAS-associated symptom that results in the admission to the hospital, whereas the clinical manifestation of FD in the first years of life is usually equivocal and probably has not been discovered by parents. Thus, comprehensive medical examinations are necessary to obtain a prompt and proper diagnosis.
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- 2021
- Full Text
- View/download PDF
5. Clinical and Hematological Relevance of JAK2V617F, CALR, and MPL Mutations in Vietnamese Patients with Essential Thrombocythemia
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Nguyen Tan Binh, Phan Thi Xinh, Huynh Nghia, Nguyen Lam Vuong, Tran Thi Thao, Cao Van Dong, Phan Nguyen Thanh Van, Hoang Anh Vu, Phu Chi Dung, and Ho Quoc Chuong
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0301 basic medicine ,Oncology ,Male ,MPL ,Essential thrombocythemia ,medicine.disease_cause ,law.invention ,Exon ,0302 clinical medicine ,law ,Medicine ,JAK2V617F ,Polymerase chain reaction ,Sanger sequencing ,Mutation ,Hematologic Tests ,General Medicine ,Middle Aged ,Prognosis ,medicine.anatomical_structure ,Vietnam ,030220 oncology & carcinogenesis ,language ,symbols ,Female ,Receptors, Thrombopoietin ,Thrombocythemia, Essential ,Research Article ,Adult ,medicine.medical_specialty ,Vietnamese ,03 medical and health sciences ,symbols.namesake ,Internal medicine ,White blood cell ,Allele-specific oligonucleotide ,Humans ,CALR ,Aged ,Retrospective Studies ,business.industry ,Janus Kinase 2 ,medicine.disease ,language.human_language ,030104 developmental biology ,business ,Calreticulin ,Follow-Up Studies - Abstract
Background: The picture of Vietnamese patients with essential thrombocythemia (ET) remains mostly undetermined. Our study intended to determine the frequency of JAK2V617F, CALR exon 9, and MPL exon 10 mutations as well as to analyze clinical characteristics associated with different mutational status in Vietnamese ET patients. Methods: We explored mutations of JAK2V617F, MPL, and CALR from 395 patients using allele specific oligonucleotide – polymerase chain reaction and Sanger sequencing techniques; then, the clinical and hematological features were compared according to mutation patterns. Results: We found that JAK2V617F, CALR exon 9, and MPL exon 10 mutations were present in 56.2%, 27.6%, and 1% of the 395 patients with ET, respectively. Twelve different types of CALR mutation were detected in 109 patients, with the CALR type 1 mutation (c.1099_1150del; L367fs*46) was the most common, followed by CALR type 2 mutation (c.1154_1155insTTGTC; K385fs*47). The JAK2V617F-positive patients had older age, higher white blood cell counts and higher hemoglobin levels but lower platelet counts than patients with CALR mutations or patients negative for triple tests. There was no significant difference regarding sex ratio, white blood cell counts, platelet counts and hemoglobin levels among CALR mutation subtypes. Conclusion: we reported high frequency of JAK2V617F, CALR, and MPL mutations in Vietnamese patients with ET and underscored the importance of combined genetic tests for diagnosis and classification of ET into different subtypes.
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- 2019
6. The Additive Cousin Problem and Related Problems for Regular Functions with Parameter Taking Values in a Clifford Algebra
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Nguyen Thanh Van and Le Hung Son
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Cousin problems ,Algebra ,Runge's theorem ,Class (set theory) ,Clifford algebra ,Cousin ,General Medicine ,Type (model theory) ,Mathematics ,Analytic function - Abstract
This article deals with the Runge type approximations problem, the solution of inhomogeneous system and the additive Cousin problem for Clifford-algebra-valued functions ƒ(x, y) which are regular with respect to x and real-analytic in y. Some main results concerning these three fundamental problems from complex analysis are proved for the class of functions mentioned above.
- Published
- 2003
- Full Text
- View/download PDF
7. Some Extension Theorems for Regular Functions of Several Quaternionic Variables
- Author
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Le Son and Nguyen Thanh Van
- Subjects
Algebra ,Quaternionic representation ,General Medicine ,Extension (predicate logic) ,Mathematics - Abstract
In this paper we study the extension theorems for solutions of inhomogeneous Cauchy-Fueter system. In particular cases, we obtain the extension theorems for regular functions of several quaternionic variables. At the end of the paper we give some applications of these theorems.
- Published
- 2002
- Full Text
- View/download PDF
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