nad has been researched along with Autosomal Dominant Myotubular Myopathy in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Beggs, AH; Buj-Bello, A; Childers, MK; Elverman, M; Goddard, MA; Grange, RW; Kelly, VE; Lawlor, MW; Mack, D; Marsh, AP; Meng, H; Poulard, K; Snyder, JM | 1 |
| Barresi, R; Bertoli, M; Burki, U; Bushby, K; Evangelista, T; Ferlini, A; Harris, E; Hudson, J; Lochmüller, H; Marini-Bettolo, C; McArthur, D; Neri, M; Polvikoski, T; Roberts, M; Scotton, C; Straub, V; Töpf, A; Vroling, B | 1 |
| Goto, K; Hayashi, YK; Ishigaki, K; Ishihara, K; Kajino, S; Nishino, I; Noguchi, S; Nonaka, I; Osawa, M | 1 |
| Fujieda, M; Matsushita, K; Murakami, N; Oishi, T; Sato, T; Takechi, T | 1 |
| Das, TK; Jain, D; Sarkar, C; Sharma, MC; Sharma, SK; Singh, S; Suri, V | 1 |
| Avila-Smirnow, D; Brochier, G; Darin, N; Fardeau, M; Lacène, E; Ohlsson, M; Oldfors, A; Quijano-Roy, S; Tajsharghi, H | 1 |
| Kontou, C; Manta, P; Papadimitriou, C; Terzis, G; Vassilopoulos, D | 1 |
7 other study(ies) available for nad and Autosomal Dominant Myotubular Myopathy
| Article | Year |
|---|---|
Long-term effects of systemic gene therapy in a canine model of myotubular myopathy.
Topics: Adenosine Triphosphatases; Animals; Dependovirus; Disease Models, Animal; Dogs; Female; Gait Disorders, Neurologic; Genetic Therapy; Glucuronidase; Humans; Longitudinal Studies; Microscopy, Electron; Muscle, Skeletal; Mutation; Myopathies, Structural, Congenital; NAD; Neurologic Examination; Protein Tyrosine Phosphatases, Non-Receptor; Respiration Disorders; Transduction, Genetic | 2017 |
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains.
Topics: Adult; Blood Platelet Disorders; Calcium; Cell Culture Techniques; DNA Mutational Analysis; Dyslexia; Erythrocytes, Abnormal; Family Health; Female; Fibroblasts; Genetic Association Studies; Humans; Ichthyosis; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Migraine Disorders; Miosis; Models, Molecular; Muscle Fatigue; Muscle, Skeletal; Mutation; Myopathies, Structural, Congenital; NAD; Neoplasm Proteins; Spleen; Stromal Interaction Molecule 1 | 2017 |
Congenital fiber type disproportion myopathy caused by LMNA mutations.
Topics: Actins; Adolescent; Child; Child, Preschool; DNA Mutational Analysis; Female; Humans; Infant; Lamin Type A; Male; Microscopy, Electron, Transmission; Muscle, Skeletal; Myopathies, Structural, Congenital; NAD; Sequence Deletion | 2014 |
[A case of X-linked myotubular myopathy with chylothorax].
Topics: Chylothorax; Humans; Infant, Newborn; Male; Myopathies, Structural, Congenital; NAD | 2016 |
Tubular aggregate myopathy: a rare form of myopathy.
Topics: Adult; Humans; Male; Middle Aged; Muscle Weakness; Muscle, Skeletal; Myopathies, Structural, Congenital; NAD; Rare Diseases; Young Adult | 2008 |
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.
Topics: Adult; Child; DNA Mutational Analysis; Female; Humans; Male; Microscopy, Electron, Transmission; Muscle, Skeletal; Mutation; Myopathies, Structural, Congenital; NAD; Photography; Tetrazolium Salts; Tropomyosin | 2008 |
Emerin expression in tubular aggregates.
Topics: Adult; AMP Deaminase; Calcium-Transporting ATPases; Cyclooxygenase 2; Humans; Hydro-Lyases; Immunohistochemistry; Isoenzymes; Male; Membrane Proteins; Microscopy, Electron; Middle Aged; Muscle, Skeletal; Muscular Dystrophy, Emery-Dreifuss; Myopathies, Structural, Congenital; NAD; Nuclear Proteins; Phosphopyruvate Hydratase; Prostaglandin-Endoperoxide Synthases; Sarcoplasmic Reticulum Calcium-Transporting ATPases; Thymopoietins | 2004 |