Vol. 3 No. 2 (2023): July-December

Editorial

Interdisciplinary Haematology

Nadeem Ikram

55-56
- PDF

Original Article

Can Different Genetic Mutations be the Possible Cause for Thrombocytosis in Children with Beta Thalassemia Major?

Mohammad Abdul Naeem, Ambreen Tauseef, Mehwish Qamar, Farhat Ijaz, Nayyar Amin

57-61
- PDF
Outcomes of Patients Treated with Brentuximab Vedotin in Relapsed or Refractory CD30 Positive Lymphomas; A Single Center Experience

Salman Arif, Natasha Ali, Usman Shaikh, Salman Adil

62-67
- PDF
Clinico-haematological Profile and Post-Induction Remission Status of Newly Diagnosed Paediatric Acute Lymphoblastic Leukaemia Patients with ETV6::RUNX1 Gene Rearrangement

Fauzia Khan, Hamid Saeed Malik, Manzar Bozdar, Rafia Mahmood, Ayesha Khurshhed, Muhammad Umar

68-73
- PDF
Correlation of FLT3 Mutation in Acute Myeloid Leukemia with Morphology and Cytogenetics

Ashja Saleem, Aiman Mahmood Minhas, Nimrah Ishaque, Jamil Awan, Rijaab Sehar, Ayisha Imran, Saadat Ali, Afaq Ahmad Nadeem

74-78
- PDF
Quantification and Frequency of Inhibitors in Congenital Coagulation Disorder Patients; An Experience at Tertiary Care Hospital

Neelam Mazhar, Shazia Yaseen, Sarah Rafi, Saima Farhan

79-83
- PDF
Outcomes of Patients with NPM1 Positive Acute Myeloid Leukemia, An Experience from a Tertiary Care Hospital in Karachi, Pakistan

Maria Zulfiqar, Natasha Ali, Usman Shaikh, Hamzah Jehanzeb, Salman Arif, Nabiha Saeed, Zurrya Fasih Khan, Zeeshan Ansar

84-88
- PDF
Protein C as an Early Indicator of Severe Coagulopathy and Mortality in Patients with Sepsis

Nimrah Ishaque, Anam Fatima Bangash, Ashja Saleem, Maryam Ramzan, Ayisha Imran, Rohma Kahookar, Ayesha Gilani

89-93
- PDF
The Role of ISTH Bleeding Assessment Tool in Diagnosing Patients with Suspected Bleeding Disorders

Aiman Minhas, Ayesha Younas, Hadia Eiman, Iqra Rasool, Mavra Fatima, Ayisha Imran, A S Chughtai

94-98
- PDF

Case Report

HaemophagocyticbLymphohistiocytosis (HLH) a Life Threatening Complication of Tuberculosis

Nadeem Ikram, Tahir Mukhtar Sayed, Fakhira Noreen, Jahanzaib Maqsood

99-103
- PDF
Acute Priapism as a First Manifestation of Chronic Phase CML; A Case Report

Nouman Nathani, Maria Zahid, Jawahar Laal, Abdul Hadi Mallick

104-106
- PDF
Refractory Autoimmune Hemolytic Anemia in a Child with Beta thalassemia Major

Aliya Batool, Sara Gilani, Sadaf Khalid, Zholdasbekova Ainur, Lawrence Faulkner, Khalid Hassan

107-110
- PDF

Letter to the Editor

Genetic Analysis of Gaucher Disease in Pakistani Population and its Diagnostic Comparison.

Qurat Abedin, Arshi Naz, Shariq ahmed, Saima Siddiqui

111-112
- PDF

Editorial

Interdisciplinary Haematology

Original Article

Can Different Genetic Mutations be the Possible Cause for Thrombocytosis in Children with Beta Thalassemia Major?

Outcomes of Patients Treated with Brentuximab Vedotin in Relapsed or Refractory CD30 Positive Lymphomas; A Single Center Experience

Clinico-haematological Profile and Post-Induction Remission Status of Newly Diagnosed Paediatric Acute Lymphoblastic Leukaemia Patients with ETV6::RUNX1 Gene Rearrangement

Correlation of FLT3 Mutation in Acute Myeloid Leukemia with Morphology and Cytogenetics

Quantification and Frequency of Inhibitors in Congenital Coagulation Disorder Patients; An Experience at Tertiary Care Hospital

Outcomes of Patients with NPM1 Positive Acute Myeloid Leukemia, An Experience from a Tertiary Care Hospital in Karachi, Pakistan

Protein C as an Early Indicator of Severe Coagulopathy and Mortality in Patients with Sepsis

The Role of ISTH Bleeding Assessment Tool in Diagnosing Patients with Suspected Bleeding Disorders

Case Report

HaemophagocyticbLymphohistiocytosis (HLH) a Life Threatening Complication of Tuberculosis

Acute Priapism as a First Manifestation of Chronic Phase CML; A Case Report

Refractory Autoimmune Hemolytic Anemia in a Child with Beta thalassemia Major

Letter to the Editor

Genetic Analysis of Gaucher Disease in Pakistani Population and its Diagnostic Comparison.

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