Oxford Index Browse

You are looking at 1-10 of 16 items for:

Haematology x Molecular Biology and Genetics x clear all

The Association of NAD(P)H:quinine Oxidoreductase Gene Polymorphisms With Pediatric Acute Lymphoblastic Leukemia

Farhad Zaker, Akram Safaei, Nahid Nasiri, Maryam Abdollahzadeh and Vahid Pazhakh.

in Laboratory Medicine

November 2012; p ublished online September 2015 .

Journal Article. Subjects: Haematology; Clinical Cytogenetics and Molecular Genetics; Molecular and Cell Biology; Molecular Biology and Genetics. 3188 words.

Objectives

Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer. NAD(P)H:quinone oxidoreductase 1 (NQO1) is an enzyme that protects cells...

Go to Oxford Journals »  home page

B Lymphoblastic Leukemia With a Novel t(11;15) (q23;q15) and Unique Burkittoid Morphologic and Immunophenotypic Findings in a 9-Year-Old Boy

Megan C. Smith, Megan K. Kressin, Eric Crawford, Xuan J. Wang and Annette S. Kim.

in Laboratory Medicine

November 2015; p ublished online November 2015 .

Journal Article. Subjects: Clinical Cytogenetics and Molecular Genetics; Haematology; Molecular and Cell Biology; Molecular Biology and Genetics. 2772 words.

B lymphoblastic leukemia is a B progenitor cell neoplasm with a range of immature immunophenotypes and several associated cytogenetic lesions. In contrast, Burkitt leukemia/lymphoma is a...

Go to Oxford Journals »  home page

G6PD Deficiency and G6PD (Mediterranean and Silent) Polymorphisms in Egyptian Infants with Neonatal Hyperbilirubinemia

Zahraa M. Ezz El-Deen, Nouran F. Hussin, Tamer A. Abdel Hamid, Osman R. Abdel Migeed and Rania M. Samy.

in Laboratory Medicine

August 2013; p ublished online September 2015 .

Journal Article. Subjects: Haematology; Clinical Cytogenetics and Molecular Genetics; Molecular and Cell Biology; Molecular Biology and Genetics. 3946 words.

Objective:

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited cause of neonatal hemolytic anemia and jaundice. We investigated...

Go to Oxford Journals »  home page

HIV-1 Viral Load Testing

Christine C. Ginocchio.

in Laboratory Medicine

March 2001; p ublished online September 2015 .

Journal Article. Subjects: Clinical Cytogenetics and Molecular Genetics; Haematology; Chemistry; Molecular and Cell Biology; Molecular Biology and Genetics. 0 words.

Go to Oxford Journals »  home page

Late Relapse of Acute Promyelocytic Leukemia: Literature Review and Results of Seven Years of Clinical and Laboratory Follow-Up of a Korean Patient

Min Jin Kim, Sun Young Cho, Hee Joo Lee, Jin-Tae Suh, Woo-In Lee, Juhie Lee, Sun Kyung Baek, Hwi-Joong Yoon and Tae Sung Park.

in Laboratory Medicine

August 2012; p ublished online September 2015 .

Journal Article. Subjects: Haematology; Clinical Cytogenetics and Molecular Genetics; Molecular and Cell Biology; Molecular Biology and Genetics. 2326 words.

Among patients with acute promyelocytic leukemia (APL), 10% to 30% experience relapse. Most relapses occur within 2 years; only a few, known as late relapses, occur 4 years after...

Go to Oxford Journals »  home page

Molecular Diagnostic Testing in Hematologic Malignancies: A Brief Overview

Daniel E. Sabath.

in Laboratory Medicine

March 2004; p ublished online September 2015 .

Journal Article. Subjects: Haematology; Clinical Cytogenetics and Molecular Genetics; Chemistry; Molecular and Cell Biology; Molecular Biology and Genetics. 0 words.

Go to Oxford Journals »  home page

Mulliken and Young's Vascular Anomalies

Edited by John B. Mulliken, Patricia E. Burrows and Steven J. Fishman.

August 2013; p ublished online November 2013 .

Book. Subjects: Surgery; Histopathology; Dermatology; History of Medicine; Paediatrics; Clinical Skills; Clinical Radiology; Surgical Skills; Molecular Biology and Genetics; Haematology; Interventional Radiology; Neurosurgery; Urology; Vascular Surgery; Trauma and Orthopaedic Surgery; Psychiatry. 812 pages.

Vascular Anomalies: Hemangiomas and Malformations is a comprehensive and interdisciplinary resource ideal for dermatologists, interventional radiologists, surgical specialists,...

Go to Oxford Medicine Online »  abstract

Primary Lymphoma of Nasal Cavity and Paranasal Sinuses

Negar Azarpira, Mohammad J Ashraf, Ahmad Monabati, Alireza Makarempour, Bijan Khademi, Afsoon Hakimzadeh, Elham Abedi and Behnaz Valibeigi.

in Laboratory Medicine

November 2012; p ublished online September 2015 .

Journal Article. Subjects: Haematology; Clinical Cytogenetics and Molecular Genetics; Molecular and Cell Biology; Molecular Biology and Genetics. 2785 words.

Background

There are several reports of lymphomas arising in the nasal cavity, either T cell/NK cell or B cell type. We studied several cases of lymphoma...

Go to Oxford Journals »  home page

Prothrombin G20210A Mutation in a 53-Year-Old Male Patient with Deep Vein Thrombosis

John Ecker and Carleen Van Siclen.

in Laboratory Medicine

February 2016; p ublished online January 2016 .

Journal Article. Subjects: Clinical Cytogenetics and Molecular Genetics; Haematology; Molecular and Cell Biology; Molecular Biology and Genetics. 1327 words.

Patient: A 53-year-old man, ethnicity unknown.

Chief Complaint: Leg swelling and pain.

History of Present Illness: The patient has a...

Go to Oxford Journals »  home page

A Rare Finding in Acute Lymphocytic Leukemia: Philadelphia Chromosome

Alyssa Taylor and Carleen Van Siclen.

in Laboratory Medicine

May 2013; p ublished online October 2015 .

Journal Article. Subjects: Haematology; Clinical Cytogenetics and Molecular Genetics; Molecular and Cell Biology; Molecular Biology and Genetics. 938 words.

Patient:

48-year-old Caucasian male

Chief Complaint:

Gastrointestinal bleeding

Medical History:null...

Go to Oxford Journals »  home page