Results
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Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit gene. [electronic resource] by
- Barisic, N
- Schmidt, C
- Sidorova, O P
- Herczegfalvi, A
- Gekht, B M
- Song, I-H
- Stucka, R
- Karcagi, V
- Abicht, A
- Lochmüller, H
Producer: 20030312
In:
Neuropediatrics vol. 33
Availability: No items available.
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[Diagnosis, surgical treatment and prognosis in patients with generalized myasthenia]. [electronic resource] by
- Kuzin, M I
- Shkrob, O S
- Gekht, B M
- Vetshev, P S
- Zaĭratíants, O V
- Kuznetsov, N S
- Chilingaridi, K E
- Voronov, L I
- Ippolitov, I Kh
- Kurochkin, A V
Producer: 19941013
In:
Khirurgiia no. 4
Availability: No items available.
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73.
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Pathogenetic therapy of diseases of the nervous system and muscles with large doses of prednisolone on alternate days. [electronic resource] by
- Gekht, B M
- Kuzin, M I
- Kolomenskaya, E A
- Gnezditskaya, E V
- Zefirova, G S
- Ibragimova, G V
- Ippolitov, I K
- Kuralesin, M G
- Polykovskaya, I D
- Shagal, D I
Producer: 19820826
In:
Neuroscience and behavioral physiology vol. 11
Availability: No items available.
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