SITI HAWA DALAM PERSPEKTIF MUHAMMAD ASAD DAN CHRISTOPH BARTH

نویسندگان

چکیده

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Siti Asmaa Mat Jusoh

Address for correspondence* Siti Asmaa Mat Jusoh Department of Hematology, School of Medical Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia. Email: [email protected]

متن کامل

Barth syndrome

Barth syndrome (BTHS) is an X-linked recessive disorder that is typically characterized by cardiomyopathy (CMP), skeletal myopathy, growth retardation, neutropenia, and increased urinary levels of 3-methylglutaconic acid (3-MGCA). There may be a wide variability of phenotypes amongst BTHS patients with some exhibiting some or all of these findings. BTHS was first described as a disease of the m...

متن کامل

Muhammad Naeem

Objective: Material and Methods:

متن کامل

Barth syndrome

First described in 1983, Barth syndrome (BTHS) is widely regarded as a rare X-linked genetic disease characterised by cardiomyopathy (CM), skeletal myopathy, growth delay, neutropenia and increased urinary excretion of 3-methylglutaconic acid (3-MGCA). Fewer than 200 living males are known worldwide, but evidence is accumulating that the disorder is substantially under-diagnosed. Clinical featu...

متن کامل

Christoph Engel

A. Introduction.......................................................................................................... 2 I. The Puzzle....................................................................................................... 2 II. The Potential for Institutions ............................................................................ 3 III. Related Approaches in Literature......

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Al-Bayan: Jurnal Studi Ilmu Al- Qur'an dan Tafsir

سال: 2019

ISSN: 2540-8461,2528-1054

DOI: 10.15575/al-bayan.v3i2.4117