scholarly journals Effect of Trauma to Primary Tooth on Permanent Maxillary Incisors: A Clinical Case Report

2017 ◽  
Author(s):  
Bhawana Gupta
Keyword(s):  
Case Report ◽  
Clinical Case ◽  
Primary Tooth ◽  
Maxillary Incisors

Apical fenestration and ectopic eruption - effects from trauma to primary tooth: a clinical case report

2010 ◽  
Vol 27 (1) ◽  
pp. 74-76 ◽  
Author(s):  
Thaisa Cezária Triches ◽  
Leonardo Koerich Paula ◽  
Marcos Ximenes Filho ◽  
Michele Bolan
Keyword(s):  
Case Report ◽  
Clinical Case ◽  
Primary Tooth ◽  
Ectopic Eruption

Clinical Case Report: Manifestation of Hereditary Neuralgic Amyotrophy in Childhood

2014 ◽  
Vol 45 (S 01) ◽  
Author(s):  
L. Voges ◽  
G. Stettner ◽  
D. Weise ◽  
K. Brockmann ◽  
J. Gärtner ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Case ◽  
Neuralgic Amyotrophy

GH/TSH secreting adenoma: a clinical case report: GH/TSH secreting adenoma: a clinical case report

2018 ◽  
Author(s):  
Tatiana Tarasova ◽  
Alexander Lutsenko ◽  
Elena Przhiyalkovskaya ◽  
Ekaterina Pigarova ◽  
Larisa Dzeranova ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Case

Designing Smile of a Worn Out Dentition - a Clinical Case Report

2012 ◽  
Vol 2 (5) ◽  
pp. 415-417
Author(s):  
Dr. Bansi M Bhusari ◽  
◽  
Dr. Shruti Sura ◽  
Dr. Kalpan Desai ◽  
Dr. Ridhima Mahajan
Keyword(s):  
Case Report ◽  
Clinical Case

Myotonic dystrophy Rossolimo-Churchman-Steinert-Batten (clinical case)

2020 ◽  
pp. 71-72
Author(s):  
И.А. Синельникова ◽  
И.В. Сопрунова ◽  
О.П. Николаева
Keyword(s):  
Case Report ◽  
Myotonic Dystrophy ◽  
Clinical Case ◽  
Molecular Genetic ◽  
Ctg Repeats ◽  
Molecular Genetic Method ◽  
Genetic Method ◽  
Family Case ◽  
Dmpk Gene

В статье представлено описание семейного случая миотонической дистрофии Россолимо-Штейнерта-Куршмана-Баттена. Диагноз подтвержден в результате ДНК-диагностики: выявлено увеличенное число копий CTG-повтора гена DMPK, ответственного за развитие миотонической дистрофии. A family case report of Rossolimo-Steinert-Curschmann myotonic dystrophy is presented. An increased number of copies of CTG-repeats of the DMPK gene responsible for the development of MD, i.e., the diagnosis was confirmed by molecular genetic method.

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