2015ء میں اشاعت کے زیور سے آراستہ ہونے والی اس نادر تحقیق کو پروفیسر عبید الحق نے مغربی بنگال کی وزیر اعلی محترمہ ممتابز جی کے ہام کیا ہے۔ (19) ۔ پرو فیسر عبد الحق نے اقبال کی نظم مسجد قرطبہ کا یہ مصرع بھی لکھا ہے ۔
خوش دل و گرم اختلاط ، ساده ورویش جبیں (20)
اور اصل اقبال کے مختصر تعارف اور کلام کے انتخاب کو مد نظر رکھ کر یہ مونوگراف تیار کیا گیا ہے۔ آج اختصار کا چلن عام ہے۔ ناول کی جگہ ناولٹ ، مقالہ کی جگہ مقالچے اور افسانے کی جگہ افسانچے کا رواج ہے۔ اس بات کو مد نظر رکھ کر فاضل مصنف نے مختصر اً اقبال کی زندگی ،کتب، فارسی اور اردو کلام پیش کیا ہے۔ مقصد یہ ہے کہ اقبالیات سے شغف رکھنے والے قاری بیزار نہ ہوں ۔
Buddhism is dominated by such other characteristics as sympathy, pity, and kindness. Furthermore, it forbids all kind of cruelty, violence, murder, brutality, and giving pain to any living creature. However, contrary to his teachings, the way his followers have targeted the Rohingya Muslims with violence and atrocities only shows how little they follow Gautama Buddha. Right from the independence of Burma, Buddhists, declaring Muslims as a threat, started their genocide, which involved attacking their mosques, their homes, dishonoring Muslim women, and harassing the Muslims without any reason. This compelled Muslims to leave their homes and migrate. The recent wave of violence, starting in June 2012, seriously affected the Muslim majority province of Arakan. Keeping in mind, Arakan is one of the fourteen Burmese provinces, where Islam have ruled since the time of Isalmic Caliphate. Unfortunately, in 1784, Burmese Prince Bodo Phia violated this garden of Islam by carrying out Muslim genocide. He banned all symbols of Islam such as pilgrimage, sacrifice, prayers, Friday and Eid Prayers, and preaching. This study points out the religious problems and issues of Muslims believers in Arakan including its impact, causes and consequences on their lives. The analytical research Methodolgy has been adopted in this studty.
Thalassemia is a hereditary quantitative deficiency of functional α and β like globin chains synthesis that leads to ineffective erythropoiesis and reduced hemoglobin synthesis. Increased gastrointestinal iron absorption, following frequent blood transfusions in the absence of proper chelation therapy, builds iron overload leading to increased morbidity and mortality and shorten life expectancy. It is manifested by chronic anemia, hepatosplenomegaly, bone deformities especially for facial bones and improper growth rate. Regular blood transfusion and iron chelation therapy becomes essential for lifelong time. The geographical distribution of thalassemia can be divided broadly into four regions: Saharan Africa, Southeast Asia, Indian Asia and Mediterranean device. Migration from these affected areas into non-malarial areas results in heterogeneous diversity of thalassemia at global level. A multicentre study (including four cities in Pakistan) was aimed to investigate the frequency and spectrum of alpha and beta thalassemia genetic mutations and XmnI polymorphism of the Gamma Globin gene. Beta thalassemia individuals identified on the ground of haematological parameters were screened for mutations of the Alpha (HBA2 and HBA1) and Beta (HBB) Globin genes as well as Gamma (HBG2) Globin gene, -158 Gg XmnI polymorphism, using a combination of multiplex GAP polymerase chain reaction (PCR), Sanger sequencing and restriction fragment length polymerase (RFLP) based PCR respectively. Among 16 identified mutations in the beta gene by Sanger sequencing, NM_000158.4:c.27_28insG (p. Ser10ValfsTer14) was the most prevalent. In alpha thalassemia mutation, multiplex GAP-PCR run for seven most common deletion mutation showed that α-3.7 and α-4.2 deletions were coinherited with beta thalassemia mutations. Additionally, presence of rare mutations and novel variants has portrait the diversity of thalassemia mutations in Pakistani population. Moreover, NM_000184.2:c.-211C>T base-pair substitution (historically described as -158 GγXmnI polymorphism) was present in 36% of the patients. The hemolysis markers (red blood cell incidences), oxidative stress (lipid peroxidation, hemoglobin oxidation, carbonyl protein oxidation, and catalase activity), antioxidative level (glutathione reduced and oxidised, scavenging assays) and biochemical parameters were also analysed. Low copper, potassium, magnesium and phosphate levels and high AST, ALK and ALT levels which were observed importantly represent the iron overloaded peroxidative state in thalassemia. Not only these parameters but high values of lipid peroxidation, carbonyl contents and catalase activity and low values of glutathione reduce and scavenging assay also marked the oxidative damage caused mainly due to iron overload and its associated complications. Additionally, three plants namely Curcuma longa (locally known as Haldi), Nigella sativa seeds (locally known as Kalonji), and Camellia sinensis (green tea) were studied to identify natural alternatives to treat disorders associated with hemolysis by reducing oxidative stress and to determine the effect of extraction systems on the functionality of phytochemicals. Based on Camellia sinensis and Curcuma longa well known bioactivities, it was assumed that they would significantly ameliorate the activities of oxidative markers and hence help in reducing the oxidative damage in beta thalassemia. However, treatment with both plant extract did not sufficiently improve the condition. This could be due to insufficient ameliorating effect as well as use of whole extract instead of isolated compound from plants was used. The psychological stress and its associated experiences were studied in index and their caregivers that duplicated the previous findings of low quality of life scores. The chronic nature of disease with enduring treatment has drastically affected their wellbeing. However, these changes vary between and within countries due to different health infrastructures, socioeconomic status and cultural and social norms. With advancement in reducing the thalassemia associated mortality and morbidity, some attention has now move into designing of improved and healthy lifestyles. Heterogeneity in clinical and haematological parameters in thalassemia major, show that monogenic disorders can present with a wide spectrum of disease severity. Present study will be useful in the prevention of highly prevalent disease of thalassemia in Pakistan following nationwide awareness campaign.