Iman M Talaat and Naglaa Mohamed Kamal
Insulin gene mutation (INS) is the second most common cause of permanent neonatal diabetes (PNDM). We present the 1st cases of Saudi monozygotic twins with permanent neonatal di..மேலும் பார்க்க»
Monireh Dashty
The LKB1/AMPK/TSC/mTORC1 cassette constitutes a canonical signaling pathway that integrates the metabolic and nutrient status of the cell for regulation of cell growth and survi..மேலும் பார்க்க»
Krisztina Lukacs, Laszlo Jozsef Barkai, Nora Hosszufalusi, Eva Palik, Attila J Szabo and Laszlo Madacsy
A case is presented of a 15-year-old boy with a past medical history of hyperlipidemia and hypertension. He attended the emergency department with a 3-day history of vomiting, a..மேலும் பார்க்க»
Tamiru Wondie, Dube Jara and Mulatu Ayana
Introduction: Macrosomia is defined as birth weight of 4,000 gm and above irrespective of gestational age and affects 3-15% of all pregnancies. Multiple factors..மேலும் பார்க்க»
Ken CN Chang*, Yun Zhao, John Kang, Saumya Pant, Ping Qiu, Bo Wei, Russell Weiner and Matthew J Marton
Use of a Next Generation Sequencing (NGS)-based test as a clinical trial assay requires that the test be analytically validated to CLIA/CAP regulations. During the course of ana..மேலும் பார்க்க»
Liliana P Paris, Yoshihiko Usui, Josefina Serino, Joaquim Sa and Martin Friedlander
Wolfram syndrome type 1 is a rare, autosomal recessive, neurodegenerative disorder that is diagnosed when insulin-dependent diabetes of non-auto-immune origin and optic atrophy ..மேலும் பார்க்க»