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101. Familial Hypocalciuric Hypercalcemia

102. Friedreich's Ataxia

103. Farber Lipogranulomatosis

104. Fructose Intolerance, Hereditary

105. Factor XI Deficiency

106. Familial Anterior Hypopituitarism

107. Familial Spastic Paraplegia

108. Frontal Temporal Lobar Degeneration

109. Familial Nonhemolytic Conjugated Hyperbilirubinemia with Normal Liver Histology

110. Familial Adenomatous Polyposis

111. Fitch Type

112. Familial Benign Hypercalcemia

113. Factor IX Deficiency

114. Familial Polymorphic Ventricular Tachycardia

115. Familial Pulmonary Arterial Hypertension

116. Familial Cortical Tremor with Epilepsy

117. Fibrofolliculomas with Trichodiscomas and Acrochordons

118. Factor V Leiden

119. Familial Ligand-defective Apolipoprotein B-100

120. Familial Combined Hyperlipidemia

121. Filiform Warts

122. Familial Startle Disease

123. Familial Cortical Myoclonic Tremor

124. Fumarylacetoacetate Hydrolase Deficiency

125. Focal Atrial Tachycardia

126. Female Pseudo-Turner Syndrome

127. Familial Benign Myoclonus Epilepsy with Adult Onset

128. Familial Renal Glucosuria

129. Functioning Sudoriparous Angiomatous Hamartoma

130. Focal Epithelial Hyperplasia

131. Functional Renal Failure

132. Fat Malabsorption

133. Familial Orthostatic Hypotensive Disorder, Streeten Type

134. Focal Proliferative Glomerulonephritis

135. Fragile X Syndrome E

136. Febrile Non-hemolytic Transfusion Reactions

137. Follicular Thyroid Cancer

138. Familial Essential Myoclonus and Epilepsy

139. Fetal Herpes Zoster Syndrome, Varicella Embryopathy

140. Functional Intestinal Obstruction

141. Familial Juvenile Hyperuricemic Nephropathy

142. Familial Hypoproteinemia with Lymphangiectatic Enteropathy

143. Flesh-Eating Syndrome

144. Factor VIII Deficiency

145. FHBL due to Apolipoprotein-B Deficiency

146. Fundus Flavimaculatus

147. Febrile Neutrophilic Dermatosis, Acute

148. Familial Juvenile Gout

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