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Procena terapijskog efekta lasera male snage i interferentnih struja kod bolesnika sa kompleksnim regionalnim bolnim sindromom primenom infracrvene termovizijske kamere.
- Published in:
- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2010, v. 67, n. 9, p. 755
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- Publication type:
- Article
Selenium toxicity: A rare diagnosis.
- Published in:
- 2016
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- Publication type:
- Case Study
Palmoplantar fibromatosis with nail dystrophy.
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2012, v. 78, n. 5, p. 646, doi. 10.4103/0378-6323.100586
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- Publication type:
- Article
Segmental vitiligo and twenty-nail dystrophy: An unusual association.
- Published in:
- 2008
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- Publication type:
- Letter
Dermatoses among paddy field workers--a descriptive, cross-sectional pilot study.
- Published in:
- 2005
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- Publication type:
- journal article
Epidermolysis bullosa pruriginosa--report of three cases.
- Published in:
- 2005
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- Publication type:
- journal article
Combined quantification of fatty infiltration, T -relaxation times and T *-relaxation times in normal-appearing skeletal muscle of controls and dystrophic patients.
- Published in:
- MAGMA: Magnetic Resonance Materials in Physics, Biology & Medicine, 2017, v. 30, n. 4, p. 407, doi. 10.1007/s10334-017-0616-1
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- Publication type:
- Article
Dystrophin-Deficient Muscular Dystrophy in aWeimaraner.
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- Journal of the American Animal Hospital Association, 2007, v. 43, n. 4, p. 227, doi. 10.5326/0430227
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- Publication type:
- Article
Biology of myospryn: what’s known?
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- Journal of Muscle Research & Cell Motility, 2008, v. 29, n. 6-8, p. 177, doi. 10.1007/s10974-008-9165-6
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- Publication type:
- Article
Fetal Akinesia Deformation Sequence and Neuroaxonal Dystrophy without PLA2G6 Mutation.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 6, p. 492, doi. 10.2350/10-01-0782-CR.1
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- Publication type:
- Article
Fetal akinesia deformation sequence and neuroaxonal dystrophy without PLA2G6 mutation.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 2, p. 1
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- Publication type:
- Article
Identification of the rare variant p.Val803Met of WFS1 gene as a cause of Wolfram-like syndrome in a Chinese family.
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- Acta Diabetologica, 2020, v. 57, n. 11, p. 1399, doi. 10.1007/s00592-020-01572-y
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- Publication type:
- Article
Histological and Ultrastructural Changes of Cardiomyocytes in Experimental Rats with Tail Thrombosis following Subplantar Application of Carrageenin.
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- Medical Principles & Practice, 2007, v. 16, n. 5, p. 360, doi. 10.1159/000104809
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- Publication type:
- Article
Viral Vectors in Gene Replacement Therapy.
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- Biochemistry (00062979), 2023, v. 88, n. 12/13, p. 2157, doi. 10.1134/S0006297923120179
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- Publication type:
- Article
基于改进自适应免疫遗传算法的智能电网虚假数据攻 击检测方法.
- Published in:
- Zhejiang Electric Power, 2023, v. 42, n. 10, p. 84, doi. 10.19585/j.zjdl.202310010
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- Publication type:
- Article
Pseudo‐psoriatic nail dystrophy revealing contact allergy to nail cosmetics.
- Published in:
- 2024
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- Publication type:
- Case Study
Selenium in the supplement as the probable cause of hair loss and nail dystrophy.
- Published in:
- 2024
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- Publication type:
- Case Study
Identification of a novel PLCD1 mutation in Chinese Han pedigree with hereditary leukonychia and koilonychia.
- Published in:
- Journal of Cosmetic Dermatology, 2019, v. 18, n. 3, p. 912, doi. 10.1111/jocd.12707
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- Publication type:
- Article
Mechanobiology and cell tensegrity: the root of ethnic hair curling?
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- Journal of Cosmetic Dermatology, 2011, v. 10, n. 2, p. 163, doi. 10.1111/j.1473-2165.2011.00553.x
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- Publication type:
- Article
Cosmetic surgery for congenital nail deformities.
- Published in:
- 2008
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- Publication type:
- Other
Concomitant Facioscapulohumeral Muscular Dystrophy and Parkinsonism Mimicking Multiple System Atrophy.
- Published in:
- Movement Disorders Clinical Practice, 2016, v. 3, n. 2, p. 194, doi. 10.1002/mdc3.12247
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- Publication type:
- Article
The role of oligodendrocyte pathology in schizophrenia.
- Published in:
- International Journal of Neuropsychopharmacology, 2007, v. 10, n. 4, p. 537, doi. 10.1017/S1461145707007626
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- Publication type:
- Article
An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report.
- Published in:
- 2007
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- Publication type:
- journal article
Cognitive impairment in adult myotonic dystrophies: a longitudinal study.
- Published in:
- Neurological Sciences, 2007, v. 28, n. 1, p. 9, doi. 10.1007/s10072-007-0742-z
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- Publication type:
- Article
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
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- Neurological Sciences, 2006, v. 27, n. 2, p. 134, doi. 10.1007/s10072-006-0615-x
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- Publication type:
- Article
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1.
- Published in:
- 2005
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- Publication type:
- journal article
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements.
- Published in:
- 2000
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- Publication type:
- journal article
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia.
- Published in:
- 2000
- By:
- Publication type:
- journal article
A case of dystrophic calcification in the masseter muscle.
- Published in:
- Maxillofacial Plastic & Reconstructive Surgery, 2017, v. 39, n. 1, p. 1, doi. 10.1186/s40902-017-0130-4
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- Publication type:
- Article
Precision Medicine and Exercise Therapy in Duchenne Muscular Dystrophy.
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- Sports (2075-4663), 2019, v. 7, n. 3, p. 64, doi. 10.3390/sports7030064
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- Publication type:
- Article
Peripheral Blood Mononuclear Cells (PB-MNCs) for the treatment of chronic tissue dystrophy in a complex case of lower limb reconstruction.
- Published in:
- European Review for Medical & Pharmacological Sciences, 2024, v. 28, n. 10, p. 3590
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- Publication type:
- Article
Choriocapillaris Flow Signal Impairment in Sorsby Fundus Dystrophy.
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- Ophthalmologica, 2022, v. 245, n. 3, p. 265, doi. 10.1159/000520931
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- Publication type:
- Article
The Survival of Donor-Derived Cells in a Successfully Grafted Corneal Button 10 Years after Penetrating Keratoplasty for Lattice Dystrophy.
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- Ophthalmologica, 2009, v. 223, n. 6, p. 396, doi. 10.1159/000228716
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- Publication type:
- Article
TGFBI Gene Mutation Analysis in Families with Hereditary Corneal Dystrophies from Ukraine.
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- Ophthalmologica, 2004, v. 218, n. 6, p. 411, doi. 10.1159/000080945
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- Publication type:
- Article
Results of an Ophthalmologic Screening Programme for Identification of Cases with Anderson-Fabry Disease.
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- Ophthalmologica, 2004, v. 218, n. 3, p. 207, doi. 10.1159/000076846
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- Publication type:
- Article
Treatment of Granular Dystrophy with Soft Contact Lenses.
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- Ophthalmologica, 2004, v. 218, n. 1, p. 70, doi. 10.1159/000074570
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- Publication type:
- Article
Filamentous tangles with nemaline rods in MYH2 myopathy: a novel phenotype.
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- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01168-9
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- Publication type:
- Article
Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy.
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- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01017-1
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- Publication type:
- Article
Autopsy case of desminopathy involving skeletal and cardiac muscle.
- Published in:
- Pathology International, 2007, v. 57, n. 1, p. 32, doi. 10.1111/j.1440-1827.2007.02053.x
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- Publication type:
- Article
Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15307-2
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- Publication type:
- Article
AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell models.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12210-8
- By:
- Publication type:
- Article
Cataract surgery in patients with Fuchs' dystrophy and corneal decompensation indicated for Descemet's membrane endothelial keratoplasty.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12434-8
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- Publication type:
- Article
Genetic characteristics of 234 Italian patients with macular and cone/cone-rod dystrophy.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07618-1
- By:
- Publication type:
- Article
White matter integrity changes and neurocognitive functioning in adult-late onset DM1: a follow-up DTI study.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07820-1
- By:
- Publication type:
- Article
Mitochondrial dysfunction associated with TANGO2 deficiency.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07076-9
- By:
- Publication type:
- Article
Causes of functional low vision in a Brazilian rehabilitation service.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-06798-0
- By:
- Publication type:
- Article
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-04817-8
- By:
- Publication type:
- Article
Altered gene expression in slc4a11<sup>−/−</sup> mouse cornea highlights SLC4A11 roles.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98921-w
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- Publication type:
- Article
Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98677-3
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- Publication type:
- Article
Characterization of SSBP1-related optic atrophy and foveopathy.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98150-1
- By:
- Publication type:
- Article