448 results on '"Sud R"'
Search Results
52. Clinical and molecular genetic studies of a cohort of Italian patients with muscle channelopathies
53. Muscle channelopathies: clinical and molecular genetic studies in a cohort of Italian patients
54. Experience with atrial fibrillation at a tertiary care centre
55. P.293 - Classic congenital myopathy with recessive mutations in genes encoding ion channels: clinical phenotype and good response to acetazolamide
56. P.229 - Skeletal muscle channelopathies: Rare treatable disorders with common presentation in childhood
57. P.230 - Large scale validation of functional expression of ClC-1 variants in genetic counselling of myotonia congenital
58. NMJ+C05 - Improving genetic diagnosis and counselling for patients with myotoniacongenita
59. NMJ+C07 - Diagnosing the undiagnosable: a targeted approach to genetic sequencingin unconfi rmed cases of skeletal muscle channelopathies
60. NMJ+C02 - Hypokalaemic periodic paralysis due to a novel ATP1A2 mutation: a new periodic paralysis gene?
61. Sofosbuvir plus ribavirin in treatment-naïve patients with chronic hepatitis C virus genotype 1 or 3 infection in India.
62. Vie, travail et santé des salariés de la sous-traitance du nucléaire
63. Proximal migration of pancreatic stent: placement of smaller stent within another stent for retrieval
64. Endoscopic ultrasound-guided fine-needle aspiration cytology in the evaluation of suspected tuberculosis in patients with isolated mediastinal lymphadenopathy
65. A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1.
66. Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype.
67. What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealed.
68. Energy dependence of the isomeric cross section ratio in the $^{58}$Ni$(n,p)^{58}$Co$^{m,g}$ reactions
69. Prevalence study of genetically defined skeletal muscle channelopathies in England
70. Germplasm appraisal of western Himalayan tea: a breeding strategy for yield and quality improvement
71. New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics
72. G.P.101 New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics
73. Analysis of the essential oil of large cardamom (Amomum subulatumRoxb.) growing in different agro-climatic zones of Himachal Pradesh, India
74. Vie, travail et santé des salariés de la sous-traitance du nucléaire
75. P39 Prevalence study of skeletal muscle channelopathies in England
76. 1154 Skeletal muscle chloride channel gene (CLCN1) copy number variation can cause myotonia congenita
77. 015 Identifying the cause of phenotypic variability in a family with non-dystrophic myotonia
78. 014 Prevalence study of skeletal muscle channelopathies in England
79. Genetic structure and diversity of India hybrid tea
80. Esophageal tuberculosis: role of endoscopic ultrasound in diagnosis
81. P30 Large scale chloride channel gene DNA rearrangements are an important cause of recessive myotonia congenitaimplications for diagnostic screening
82. P24 Genetic heterogeneity and mechanisms of phenotypic variability in human skeletal muscle channelopathies – a new S4 mutation not associated with HypoPP
83. Endoscopic ultrasound-guided fine-needle aspiration cytology in the evaluation of suspected tuberculosis in patients with isolated mediastinal lymphadenopathy
84. P91 Using MRI as a diagnostic tool in the skeletal muscle channelopathies
85. P43 Acetazolamide response in patients affected by hypokalemic periodic paralysis
86. A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A
87. Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
88. Salvage therapy for relapsed or refractory diffuse large B-cell lymphoma: impact of prior rituximab
89. What causes paramyotonia in the United Kingdom?: Common and new SCN4A mutations revealed
90. Transcriptosome Profiling of B-CLL Identifies WNT-3A and ROR-1 as an Autocrine Mechanism in Cell Survival.
91. The dissipation of neuropathic pain paradoxically involves the presence of tumor necrosis factor-? (TNF)
92. An antidepressant mechanism of desipramine is to decrease tumor necrosis factor-α production culminating in increases in noradrenergic neurotransmission
93. P0817 CLINICAL PROFILE OF PANCREATIC DISORDERS IN CHILDREN IN NORTH INDIA
94. O0095 ROLE OF ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY IN THE MANAGEMENT OF PANCREATITIS IN CHILDREN
95. VIISta 810 dosimetry performance.
96. Cell Lineage of Vein Formation in Variegated Leaves of the C4Grass Stenotaphrum secundatum
97. Control of Lantana in non-cropped area and in tea plantation
98. Molecular and cytogenetic investigation of the DCC gene in colorectal cancer
99. Infrequent alterations of the APC and MCC genes in gastric cancers from British patients
100. Molecular characterisation of an 8P minichromosome that includes the site of a tumour suppressor gene
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.