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103. Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families

104. Comprehensive Genetic Analysis of 182 Unrelated Families with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

105. Psychiatric characterization of children with genetic causes of hyperandrogenism

106. A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency

108. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline

109. The Phenotypic Spectrum of Contiguous Deletion of CYP21A2 and Tenascin XB: Quadricuspid Aortic Valve and Other Midline Defects

110. A pharmacokinetic and pharmacodynamic study of delayed- and extended-release hydrocortisone (Chronocort) vs. conventional hydrocortisone (Cortef) in the treatment of congenital adrenal hyperplasia

111. Early hyperandrogenism affects the development of hippocampal function: preliminary evidence from a functional magnetic resonance imaging study of boys with familial male precocious puberty

112. Modified-release hydrocortisone to provide circadian cortisol profiles

113. Quality of life in children and adolescents 1-year after cure of Cushing syndrome: a prospective study

114. Selective IgA Deficiency

115. Stargardt Disease

116. Smokers' Lung

117. SMCD

118. SAP-Precursor Deficiency

119. Systolic Click-Murmur Syndrome

120. Subcutaneous Panniculitis-like T-Cell Lymphoma

121. Spina Bifida

122. Sly Syndrome

123. SRPS Type I

124. Secondary Aldosteronism

125. Supernumerary Nipple(s)

126. Symptomatic Partial Epilepsy

127. Sulfatide Activator Deficiency

128. Seasonal Perennial Conjunctivitis

129. Spinal Spastic Paraplegia

130. Signal Transduction of Apoptosis

131. Stress-induced Tachycardia

132. Supraventricular Tachycardia

133. Spondyloepiphyseal Dysplasia Tarda

134. Shah-Waardenburg Syndrome

135. Slowing of Respiration

136. Sphingolipid Activator Protein Deficiency

137. Spinocellular Carcinoma

138. Subacute Nonsuppurative Thyroiditis

139. Spondyloepiphyseal Dysplasia Congenita

140. Stress-induced Polymorphic Ventricular Tachycardia

141. Severe Myoclonic Epilepsy of Infancy

142. Subepithelial Mucinous Corneal Dystrophy

143. Sarcoid Myositis

144. Slow-Transit Constipation

145. Subtype of Nemaline Myopathies or NEM3

146. Sexual Precocity

147. Stiff Person Syndrome

148. Sodium Channel Myotonia

149. Slipped Capital Femoral Epiphysis

150. Slow Ventricular Tachycardia

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