644 results on '"Lin, Hsiang-Yu"'
Search Results
102. Epidemiological evolution of early-onset neonatal sepsis over 12 years: A single center, population-based study in central Taiwan.
103. Detection of hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: Biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers
104. Functional independence of Taiwanese children with VACTERL association
105. Activation of silenced tumor suppressor genes in prostate cancer cells by a novel energy restriction-mimetic agent
106. Molecular basis of mucopolysaccharidosis type IVA (Morquio syndrome type A): A review and classification of gene variants and reporting of new variants
107. Incidence and treatment of adult femoral fractures with osteogenesis imperfecta: An analysis of a center of 72 patients in Taiwan
108. Otorhinolaryngological Management in Taiwanese Patients with Mucopolysaccharidoses
109. Genetic Studies of Prader-Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q
110. Aortic Root Dilatation in Taiwanese Patients with Mucopolysaccharidoses and the Long-Term Effects of Enzyme Replacement Therapy
111. Effect of Mutated ids Overexpression on IDS Enzyme Activity and Developmental Phenotypes in Zebrafish Embryos: A Valuable Index for Assessing Critical Point-Mutations Associated with Mucopolysaccharidosis Type II Occurrence in Humans
112. Taiwan's experience of otorhinolaryngological management in patients with mucopolysaccharidoses
113. Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985-2019)
114. Polysomnographic Characteristics in Patients With Mucopolysaccharidoses
115. Incidence of the Mucopolysaccharidoses in Taiwan, 1984–2004
116. Airway Management of the Deformed Trachea Using T-Tube Stents in Patients with Mucopolysaccharidosis Type IVA.
117. Polysomnographic Characteristics in Patients With Prader-Willi Syndrome
118. Prenatal Sonographic Findings of Klippel-Tré;naunay-Weber Syndrome
119. Prader–Willi syndrome in Taiwan
120. Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985–2004
121. Genotype and phenotype in patients with Prader–Willi Syndrome in Taiwan
122. Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988–2004
123. The first mucopolysaccharidosis type VII in a Taiwanese girl: A case report and review of the literature.
124. Esophageal Perforation: A Complication of Nasogastric Tube Placement in Premature Infants
125. Population based retrospective cohort study on risk of retinopathy of prematurity in twins
126. FADS Genetic Variants in Taiwanese Modify Association of DHA Intake and Its Proportions in Human Milk
127. Cardiac Evaluation Using Two-Dimensional Speckle-Tracking Echocardiography and Conventional Echocardiography in Taiwanese Patients with Mucopolysaccharidoses
128. Identification and Functional Characterization of IDS Gene Mutations Underlying Taiwanese Hunter Syndrome (Mucopolysaccharidosis Type II)
129. Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan
130. Relationships among Height, Weight, Body Mass Index, and Age in Taiwanese Children with Different Types of Mucopolysaccharidoses
131. Long-term outcomes of enzyme replacement therapy for Taiwanese patients with Mucopolysaccharidosis I
132. Functional independence of Taiwanese patients with mucopolysaccharidoses
133. Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVA
134. A Truncating De Novo Point Mutation in a Young Infant with Severe Menkes Disease
135. Ophthalmologic manifestations in Taiwanese patients with mucopolysaccharidoses
136. Awareness of attenuated mucopolysaccharidoses in a pediatric orthopedic clinic
137. Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery in an Infant
138. Erratum to: Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan
139. The relationships between urinary glycosaminoglycan levels and phenotypes of mucopolysaccharidoses
140. Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21‐year period
141. Functional independence of Taiwanese children with Prader-Willi syndrome
142. Factors That Influence Human Milk Feeding at Hospital Discharge for Preterm Infants in a Tertiary Neonatal Care Center in Taiwan
143. Molecular basis of mucopolysaccharidosis type IVA (Morquio syndrome type A): A review and classification of GALNS gene variants and reporting of new variants
144. Infected cephalohaematoma with serious complications: Is it preventable?
145. AB036. Cardiac features in Taiwanese patients with mucopolysaccharidosis IVA
146. Bio-Plex immunoassay measuring the quantity of lysosomal N -acetylgalactosamine-6-sulfatase protein in dried blood spots for the screening of mucopolysaccharidosis IVA in newborn: a pilot study
147. Awareness of Mucopolysaccharidosis in an Otorhinolaryngologic Clinic
148. AB164. Methylmalonic acidemia/propionic acidemia in Taiwan
149. AB084. Cause of death and clinical characteristics of 34 mortality patients with mucopolysaccharidosis II in Taiwan, 1995-2012
150. AB108. The appliance of Bio-Plex immunoassay using dried blood spots for mucopolysaccharidosis IVA newborn screening in Taiwan—a pilot study
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