424 results on '"Milla C"'
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52. EARLY MINNESOTA CYSTIC FIBROSIS MEWBORN SCREENING OUTCOMES AT THE UNIVERSITY OF MINNESOTA AND THE INCORPORATION OF GENETIC COUNSELING: 186
53. From Page to Performance: Essays in Early English Drama
54. Ta'ziyeh in exile: transformations in a Persian tradition
55. Primary ciliary dyskinesia: Longitudinal study of lung disease by ultrastructure defect and genotype
56. Síntesis Directa de Ciclobutenonas desde Yodoalquinos Catalizada por Paladio
57. WS07-5 Lack of correlation between patient reported outcomes (PROs) and Lung Clearance Index (LCI2.5) among cystic fibrosis children with normal spirometry
58. WS06-2 Initial results evaluating the add-on effect of the novel CFTR corrector PTI-801 in cystic fibrosis subjects
59. WS12-4 Long-term safety and efficacy of lumacaftor/ivacaftor therapy in patients aged 6–11 years with cystic fibrosis homozygous for the F508del-CFTR mutation (F/F)
60. Homer1 Is Increased in Idiopathic Pulmonary Fibrosis and Affects Fibroblasts Behavior
61. PCR ribotyping and endonuclease subtyping in the epidemiology of Burkholderia cepacia infection.
62. FUNGUS AMONG US: AVAILABLE TESTS FOR MOLD-PRODUCED MYCOTOXINS IN THE USA AND THEIR CLINICAL RELEVANCE
63. Transition metal-free controlled synthesis of bis[(trifluoromethyl)sulfonyl]ethyl-decorated heterocycles
64. Preschool multiple-breath washout testing an official American Thoracic Society technical statement
65. Evolution After Anti-TNF Discontinuation in Patients With Inflammatory Bowel Disease: A Multicenter Long-Term Follow-Up Study
66. Visualizing the Moral Life: Medieval Iconography and the Macro Morality Plays
67. When the City is Your Classroom
68. Food consumption based on processing level (according to Nova system) during the COVID-19 pandemic among adolescents with immunocompromised conditions: a case-control study
69. Biallelic variants in genes previously associated with dominant inheritance: CACNA1A, RETand SLC20A2
70. Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype
71. WS11.3 Longitudinal assessment of sweat chloride values among infants identified by newborn screening
72. 43 Clinical benefit of ivacaftor on a patient with 3849+10 kb C>T CFTR mutation
73. A Existência de um Estado de Coisas Inconstitucional em Matéria Ambiental
74. Osteomalacia oncogênica: a perda de fosfatemia pode ser a chave para evitar o diagnóstico incorreto
75. Ta'ziyeh in Exile: Transformations in a Persian Tradition
76. Metal-free [3+2] cycloaddition of azides with Tf2CCH2 for the regioselective preparation of elusive 4-(trifluoromethylsulfonyl)-1,2,3-triazoles
77. Unveiling the uncatalyzed reaction of alkynes with 1,2-dipoles for the room temperature synthesis of cyclobutenes
78. Multiple-breath washout as a lung function test in cystic fibrosis: A cystic fibrosis foundation workshop report
79. Changes in Eating Habits and Sedentary Behavior During the COVID-19 Pandemic in Adolescents With Chronic Conditions
80. 40 Longitudinal values of sweat chloride concentration among infants identified by cystic fibrosis (CF) newborn screening (NBS) in California
81. 215 Comparison of acute effects of conventional high frequency chest oscillation (HFCWO) and hand held percussor (Electro-Flo 5000) for airway clearance in cystic fibrosis patients
82. Oncogenic osteomalacia: loss of hypophosphatemia might be the key to avoid misdiagnosis
83. P365 Effectiveness of adalimumab in the treatment of perianal fistulas in patients with Crohn's disease naïve to anti-TNF: A multicenter study
84. P340 Has the risk of developing colorectal cancer in patients with ulcerative colitis been overstated? A meta-analysis
85. When the City is Your Classroom
86. CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR
87. Sweat chloride (SC) concentration and CFTR mutation class among infants identified by newborn screening (NBS) in California (CA)
88. Pre-transplant risk factors affecting outcome in Hurler syndrome
89. A Phase I/II Study of the Anti-PcrV Antibody KB001 in Cystic Fibrosis Patients with Pseudomonas aeruginosa.
90. Influence of Body Mass Index on Eating Habits and Food Choice Determinants Among Brazilian Women During the COVID-19 Pandemic
91. Influence of Cutting Fluid Application Frequency in Micromilling Cutting Forces
92. Poor Eating Habits and Selected Determinants of Food Choice Were Associated With Ultraprocessed Food Consumption in Brazilian Women During the COVID-19 Pandemic
93. Of Genes and Men: The Alternative View of Sex Differences in Cystic Fibrosis: Response to Creus et al.
94. Análise de indicadores de desempenho da manutenção de um moinho de bolas
95. Long term effects of aerosolised rhDNase on pulmonary disease progression in patients with cystic fibrosis
96. Comparison of settings used for high-frequency chest-wall compression in cystic fibrosis.
97. Insulin and glucose excursion following premeal insulin lispro or repaglinide in cystic fibrosis-related diabetes.
98. Protein metabolism in clinically stable adult cystic fibrosis patients with abnormal glucose tolerance.
99. Geraldo Andrew Vieira.
100. Peter Minshall.
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