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101. Hereditary Renal Hypouricemia

102. Myocardial Infarction, Acute

103. Mucous Membrane Pemphigoid

104. Primary Carnitine Deficiency

105. Primary Sclerosing Cholangitis

106. MPS IV

107. Pulmonary Hypertension

108. Moniliform Hair

109. Phosphorylase B Kinase Deficiency

110. Shock Liver

111. Spinocellular Carcinoma

112. Primary Open Angle Glaucoma

113. Metabolic Syndrome

114. Hepatitis, Acute

115. Pseudohypoaldosteronism Type II

116. Pulmonary Atresia with Ventricular Septal Defect

117. Pharyngoesophageal Diverticula

118. Subacute Nonsuppurative Thyroiditis

119. Hauptmann-Thannhauser Muscular Dystrophy

120. Purpura Schoenlein-Henoch

121. Spondyloepiphyseal Dysplasia Congenita

122. Stress-induced Polymorphic Ventricular Tachycardia

123. High Triglycerides

124. Hemophilia B

125. Human RSV

126. Mixed Connective Tissue Disease

127. Partial Androgen Insensitivity Syndrome

128. Hypotrichosis-Lymphedema-Telangiectasia Syndrome

129. Severe Myoclonic Epilepsy of Infancy

130. Hypertrophic Pulmonary Osteoarthropathy

131. Sarcoid Myositis

132. Subepithelial Mucinous Corneal Dystrophy

133. Primary Cutaneous Anaplastic Large-Cell Lymphoma

134. Primary Pulmonary Hypertension

135. Hyperostosis Calvaria Interna

136. Monosodium Urate Crystal Deposition Disease

137. Hyperlipoproteinemia Type Ib

138. McCune-Albright Syndrome

139. Slow-Transit Constipation

140. Pott’s Disease (Spine)

141. Subtype of Nemaline Myopathies or NEM3

142. Hypocalcemia with Hypercalciuria, Autosomal Dominant

143. Hemosiderosis, Idiopathic Pulmonary

144. Hypovitaminosis E

145. Sexual Precocity

146. Methylenetetrahydrofolate Reductase Deficiency

147. Hereditary Breast and Ovarian Carcinoma

148. Homocystinuria due to Cystathionine Beta-Synthase Deficiency

149. Pelizaeus-Merzbacher Disease

150. Pityriasis Simplex Faciei

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