1,407 results on '"MAYATEPEK, Ertan"'
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52. Adressen
53. Stoffwechselerkrankungen
54. BCG Vaccination-Associated Lower HbA1c and Increased CD25 Expression on CD8 + T Cells in Patients with Type 1 Diabetes in Ghana.
55. Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability
56. Trimethylaminuria, Dimethylglycine Dehydrogenase Deficiency and Disorders in the Metabolism of Glutathione
57. Resilience strengthening in youth with a chronic medical condition- a randomized controlled feasibility trial of a combined app and coaching program
58. Dentale Vernachlässigung: Ein Instrument zur Identifikation und multisektoralen Kooperation im präventiven Kinderschutz
59. Combination of Ileal bile acid transporter inhibitor and a non-steroidal Farnesoid X receptor agonist for reversal of cholestatic liver injury in Cyp2c70 KO mice with a humanized bile acid composition
60. 11 - Stoffwechselerkrankungen
61. Kapitel 7 - Stoffwechselerkrankungen
62. Kapitel 2 - Vorsorgeuntersuchungen
63. Kapitel 1 - Anamnese, Untersuchung, Arbeitstechniken und Besonderheiten im Umgang mit Patienten und Eltern
64. Cooperative role of lymphotoxin β receptor and tumor necrosis factor receptor p55 in murine liver regeneration
65. Correction to: The antioxidant Trolox restores mitochondrial membrane potential and Ca2+-stimulated ATP production in human complex I deficiency
66. Vorwort
67. Vorsorgeuntersuchungen
68. Stoffwechselerkrankungen
69. Anamnese, Untersuchung, Arbeitstechniken und Besonderheiten im Umgang mit Patienten und Eltern
70. Assessment of retinopathy of prematurity regression and reactivation using an artificial intelligence–based vascular severity score
71. Monocyte pathology in human tuberculosis is due to plasma milieu changes and aberrant STAT signalling
72. BCG-Vaccinated Children with Contact to Tuberculosis Patients Show Delayed Conversion of Mycobacterium tuberculosis-Specific IFN-γ Release
73. Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders
74. Late-Onset Group B Streptococcal Meningitis Has Cerebrovascular Complications
75. Lipoprotein-associated phospholipase A2 activity in obese adolescents with and without type 2 diabetes
76. Alternative Quantiferon cytokines for diagnosis of children with active tuberculosis and HIV co-infection in Ghana
77. Screening for non-alcoholic fatty liver disease in children and adolescents with type 1 diabetes mellitus: a cross-sectional analysis
78. Biotin-Responsive Basal Ganglia Disease: A Treatable Differential Diagnosis of Leigh Syndrome
79. Störungen des Aminosäurenstoffwechsels
80. Leukotrienes
81. Delayed-Onset Transient Hyperinsulinism in Infants with Very Low and Extremely Low Birth Weights: A Cohort Study
82. Disorders in the Metabolism of Glutathione and Imidazole Dipeptides
83. Immunological Problems
84. Psychiatric Disease
85. Neonatal encephalocardiomyopathy caused by mutations in VARS2
86. Disorders of Mitochondrial Fatty Acid Oxidation and Related Metabolic Pathways
87. The many faces of paediatric mitochondrial disease on neuroimaging
88. Genetic cause and prevalence of hydroxyprolinemia
89. EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosum
90. IL-1RA Antibodies in Myocarditis after SARS-CoV-2 Vaccination
91. Association of Household Deprivation, Comorbidities, and COVID-19 Hospitalization in Children in Germany, January 2020 to July 2021
92. T-Cell Responses Against Mycobacterium ulcerans and Mycobacterium tuberculosis Protein Extracts Identify Children With Buruli Ulcer Disease
93. Leukotrienes
94. Characterization of pancreatic NMDA receptors as possible drug targets for diabetes treatment
95. Post stroke hemi-dystonia in children: a neglected area of research
96. MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy
97. Adressen
98. Stoffwechselerkrankungen
99. MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities
100. Treatment options for lactic acidosis and metabolic crisis in children with mitochondrial disease
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