J. Poole

发表

NEONATAL HAEMOLYTIC ANAEMIA- A DIAGNOSTIC APPROACH TO RED CELL MEMBRANE DISORDERS

T. Coetzer, L. Swart, K. Naidoo, 2018, South African Journal of Child Health.

Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.

A. Krause, J. Poole, T. Haw, 2015, Blood cells, molecules & diseases.

Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation

A. Krause, C. Sutton, J. Poole, 2013, Genetics in Medicine.

Malignant Liver Tumors in South African Children: A National Audit

S. Moore, M. Kruger, G. Hadley, 2008, World Journal of Surgery.

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.

C. Lewis, C. Mathew, T. de Ravel, 2000, Blood.

Infection with human immunodeficiency virus‐1 (HIV) among children with cancer in South Africa

R. Newton, J. Poole, G. Wessels, 2011, Pediatric blood & cancer.

Malignancies in South African Children With HIV

M. Kruger, D. Reynders, M. Hendricks, 2014, Journal of pediatric hematology/oncology.

Hepatocellular carcinoma and liver tumors in South African children

S. Moore, M. Kruger, G. Hadley, 2004, Cancer.

Determinants of survival in children with cancer in Johannesburg, South Africa

J. Geel, J. Poole, Nadia Beringer, 2021, South African Journal of Oncology.

Pattern of 6‐Mercaptopurine Urinary Excretion in Children with Acute Lymphoblastic Leukemia: Urinary Assays as a Measure of Drug Compliance

J. Poole, L. Macdougall, Elaine Ross, 1992, Therapeutic Drug Monitoring.

A 20-Year Retrospective Review of Retinoblastoma at Two Tertiary Academic Hospitals in Johannesburg, South Africa

J. Poole, I. Mayet, L. Wainwright, 2017, Ocular Oncology and Pathology.

The Saint Siluan warning signs of cancer in children: Impact of education in rural South Africa

J. Poole, L. Wainwright, D. Mackinnon, 2011, Pediatric blood & cancer.

Beta-thalassaemia--the Johannesburg experience.

J. Poole, R. Cohn, H. Roode, 1989, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

A common Fanconi anemia mutation in black populations of sub-Saharan Africa.

C. Lewis, C. Mathew, T. de Ravel, 2005, Blood.

The implementation of a national paediatric oncology protocol for neuroblastoma in South Africa

M. Kruger, J. van Heerden, M. Hendricks, 2021, Cancer Causes & Control.

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.

Marion E. Schneider, B. Fadeel, C. Söderhäll, 2001, American journal of human genetics.

Granulocytic sarcoma in children with acute myeloblastic leukemia and t(8;21).

J. Poole, G. Sherman, R. Cohn, 1998, Medical and pediatric oncology.

Recommendations for the management of sickle cell disease in South Africa.

N. Alli, J. Poole, M. Coetzee, 2014, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

The pre-surgical factors that determine the decision to proceed to resection in children diagnosed with high-risk neuroblastoma in a resource limited setting.

M. Kruger, J. van Heerden, T. Esterhuizen, 2022, Pediatric hematology and oncology.

Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.

A. Vral, J. Slabbert, K. De Leeneer, 2018, DNA repair.

Compound heterozygous sickle cell disease and β0-thalassaemia: An interesting case

N. Alli, J. Poole, R. Schwyzer, 2013 .

Incidence of AIDS-defining and Other Cancers in HIV-positive Children in South Africa: Record Linkage Study

M. Egger, B. Eley, J. Bohlius, 2016, The Pediatric infectious disease journal.

Management of undifferentiated embryonal sarcoma of the liver in children: a case series and management review.

P. Beale, J. Geel, J. Poole, 2013, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.

A. Krause, J. Poole, T. Wainstein, 2013, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Posterior neck mass in a four-year-old boy.

J. Poole, I. Friedland, M. John, 1995, The Pediatric infectious disease journal.

Comparative study of Fanconi anemia in children of different ethnic origin in South Africa.

J. Poole, L. Macdougall, J. Rosendorff, 1994, American journal of medical genetics.

sub-Saharan Africa A common Fanconi anemia mutation in black populations of

C. Lewis, C. Mathew, I. Demuth, 2013 .

CD10 antigen density in childhood common acute lymphoblastic leukaemia: comparisons of race and sex.

B. Mendelow, J. Poole, D. Glencross, 1992, Leukemia research.

An interinstitutional review of the value of FNAB in pediatric oncology in resource‐limited countries

M. Louw, P. Schubert, C. Wright, 2012, Diagnostic cytopathology.

Paediatric cancer survivors demonstrate a high rate of subclinical renal dysfunction

J. Geel, J. Poole, Abdullahi Mudi, 2016, Pediatric blood & cancer.

Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation

A. Krause, D. Reynders, J. du Plessis, 2020, Molecular genetics & genomic medicine.

α‐interferon therapy for severe chronic idiopathic thrombocytopenic purpura in children

P. Hesseling, J. Poole, R. Cohn, 1993 .

Childhood cancer incidence in South Africa, 1987-2007.

E. Steliarova-Foucher, D. Forman, M. Colombet, 2015, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Age at diagnosis as a prognostic factor in South African children with neuroblastoma

M. Kruger, J. van Heerden, T. Esterhuizen, 2021, Pediatric blood & cancer.

Bilateral Wilms’ tumour: A ten-year experience of two academic centres in Johannesburg

J. Poole, J. Loveland, R. Wainwright, 2021 .

Extranodal presentation of a lymphoma with precursor B-cell phenotype and translocation t(8;14) in South Africa

T. Wiggill, J. Poole, D. Glencross, 1970, African journal of laboratory medicine.