582 results on '"Touraine Philippe A."'
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102. Vulvar Lichen Sclerosus Is Very Frequent in Women With Turner Syndrome
103. Normal spermatogenesis in a man with mutant luteinizing hormone
104. Travelling in time and space in the heart of Paris
105. Hypogonadotropic hypogonadism revealing a classic form of 21 hydroxylase deficiency in a 39 year old man
106. Infertility revealing a classical form of congenital adrenal hyperplasia in a 39 years old man
107. Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21‑hydroxylase deficiency in Europe
108. Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
109. Editorial: Travelling in time and space in the heart of Paris
110. Modified-Release Hydrocortisone in Congenital Adrenal Hyperplasia
111. Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe
112. Benign Breast Diseases
113. Next Generation Sequencing Should Be Proposed to Every Woman With “Idiopathic” Primary Ovarian Insufficiency
114. Effects of mitotane on testicular adrenal rest tumors in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a retrospective series of five patients
115. Puberty and fertility in classic galactosemia
116. Coordinateurs
117. Study of Anti-Müllerian Hormone and Its Relation to the Subsequent Probability of Pregnancy in 112 Patients With Systemic Lupus Erythematosus, Exposed or Not to Cyclophosphamide
118. Primary Adrenal Insufficiency Due to Bilateral Adrenal Hemorrhage-Adrenal Infarction in the Antiphospholipid Syndrome: Long-Term Outcome of 16 Patients
119. NR5A1 (SF-1) Mutations Are Not a Major Cause of Primary Ovarian Insufficiency
120. LH Pulsatility and Secretion Are Tightly Associated with Hormonal Control in CAH Patients
121. Identification of Gain-of-Function Variants of the Human Prolactin Receptor
122. Syndrome d’Ehlers-Danlos vasculaire
123. Human prolactin (hPRL) antagonists inhibit hPRL-activated signaling pathways involved in breast cancer cell proliferation
124. Is prolactin involved in the evolution of atherothrombotic disease?
125. Markers of Recurrence and Long-Term Morbidity in Craniopharyngioma: A Systematic Analysis of 171 Patients
126. Modified-Release Hydrocortisone in Congenital Adrenal Hyperplasia
127. Transition of young adults with endocrine and metabolic diseases: the ‘TRANSEND’ cohort
128. Resumption of Ovarian Function and Pregnancies in 358 Patients with Premature Ovarian Failure
129. Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort
130. Novel anti-mullerian hormone mutation revealed by haematospermia in a 60-year-old patient
131. Studying the care and social pathway of young adults with endocrine and metabolic diseases during transition: The ‘Transend’ cohort
132. GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
133. Positive association between progestins and the evolution of multiple fibroadenomas in 72 women
134. MON-LB308 Studying the Care and Social Pathway of Young Adults With Endocrine and Metabolic Diseases During Transition: The “Transend” Cohort
135. Premature ovarian insufficiency: step-by-step genetics bring new insights
136. OR25-02 A Phase 3 Study of a Modified-Release Hydrocortisone in the Treatment of Congenital Adrenal Hyperplasia
137. Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
138. Characterization of Two Constitutively Active Prolactin Receptor Variants in a Cohort of 95 Women with Multiple Breast Fibroadenomas
139. FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report
140. Hormonal replacement therapy in menopausal women with a history of hyperprolactinemia
141. Clinical and Molecular Characterization of a Cohort of 161 Unrelated Women with Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and 330 Family Members
142. Quand et comment traiter une hyperprolactinémie ?
143. Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency.
144. Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management.
145. Premature ovarian failure: predictability of intermittent ovarian function and response to ovulation induction agents
146. Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea
147. Bilateral Adrenal Infiltration in Erdheim-Chester Disease. Report of Seven Cases and Literature Review
148. Chapitre 36 - Hyperandrogénie d'origine ovarienne
149. A New Mechanism for Prolactin Processing into 16K PRL by Secreted Cathepsin D
150. Drug Insight: prolactin-receptor antagonists, a novel approach to treatment of unresolved systemic and local hyperprolactinemia?
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