| Issue |
Section |
Title |
File |
| Vol 4, No 1 (2014) |
CLINICAL DISCUSSION |
Late-onset Pompe disease: first clinical description in Russia |
(Rus)
|
| Vol 3, No 3 (2013) |
CLINICAL DISCUSSION |
Infantile-onset Pompe disease (the first case diagnosed in Voronezh) |
(Rus)
|
| Vol 2, No 4 (2012) |
CLINICAL DISCUSSION |
Infantile Pompe disease: Clinical picture, diagnosis, and treatment |
(Rus)
|
| Vol 5, No 2 (2015) |
CLINICAL DISCUSSION |
Differential diagnosis of mitochondrial neurogastrointestinal encephalomyopathy. First clinical description in Russia |
(Rus)
|
| Vol 5, No 3 (2015) |
CLINICAL DISCUSSION |
Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy |
(Rus)
|
| Vol 6, No 1 (2016) |
LECTURES AND REVIEWS |
Clinical Practice Guidelines for delivery of healthcare to patients with Pompe disease |
(Rus)
|
| Vol 9, No 3 (2019) |
CLINICAL DISCUSSION |
Infantile and early childhood onset of mitochondrial myopathy due to mutations in the TK2 gene with a phenotype of spinal muscular atrophy 5q: the first cases in Russia |
(Rus)
|
| Vol 11, No 2 (2021) |
CLINICAL DISCUSSION |
Glutaric aciduria type 1 in children. Clinical presentation of 46 cases in Russian families |
(Rus)
|
| Vol 11, No 4 (2021) |
LECTURES AND REVIEWS |
Practical aspects of therapy for glutaric aciduria type 1 |
(Rus)
|
| Vol 12, No 2 (2022) |
ORIGINAL REPORTS |
Differential diagnosis of myopathy and multiple epiphysal dysplasia caused by mutations in the COMP gene in children |
(Rus)
(Eng)
|
