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"I'm still dad": The Impact of Scleroderma on being a Father

Occupational therapy in health care, 2018-01, Vol.32 (1), p.1-13

2018

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Parenting: the forgotten role of women living with systemic lupus erythematosus

Clinical rheumatology, 2012-06, Vol.31 (6), p.995-1000

2012

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

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1351-n/a

2020

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Measuring Dexterity in Children Using the Nine-hole Peg Test

Journal of hand therapy, 2005-07, Vol.18 (3), p.348-351

2005

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Occupation of motherhood: challenges for mothers with scleroderma

The American journal of occupational therapy, 2009-03, Vol.63 (2), p.214

2009

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Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

American journal of human genetics, 2001-03, Vol.68 (3), p.590-597

2001

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Perceived Parenting Ability and Systemic Sclerosis

Musculoskeletal care, 2011-03, Vol.9 (1), p.32-40

2011

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Effect of Wrist Hand Splints on Grip, Pinch, Manual Dexterity, and Muscle Activation in Children with Spastic Hemiplegia: A Preliminary Study

Journal of hand therapy, 2008, Vol.21 (1), p.36-43

2008

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Paediatric cancer survivors demonstrate a high rate of subclinical renal dysfunction

Pediatric blood & cancer, 2016-11, Vol.63 (11), p.2026-2032

2016

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

The Pediatric infectious disease journal, 2016-06, Vol.35 (6), p.e164-e170

2016

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

Pediatric hematology and oncology, 2023-04, Vol.40 (3), p.242-257

2023

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Micafungin Versus Liposomal Amphotericin B for Pediatric Patients With Invasive Candidiasis: Substudy of a Randomized Double-Blind Trial

The Pediatric infectious disease journal, 2008-09, Vol.27 (9), p.820-826

2008

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

Blood cells, molecules, & diseases, 2015-03, Vol.54 (3), p.270-274

2015

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

Genetics in medicine, 2014-05, Vol.16 (5), p.400-406

2014

Volltextzugriff (PDF)

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

Pediatric blood & cancer, 2011-02, Vol.56 (2), p.314-316

2011

Volltextzugriff (PDF)

Malignancies in South African children with HIV

Journal of pediatric hematology/oncology, 2014-03, Vol.36 (2), p.111-117

2014

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

Pediatric blood & cancer, 2011-01, Vol.56 (1), p.77-79

2011

Volltextzugriff (PDF)

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

Diagnostic cytopathology, 2012-09, Vol.40 (9), p.770-776

2012

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Hepatocellular carcinoma and liver tumors in South African children: A case for increased prevalence

Cancer, 2004-08, Vol.101 (3), p.642-649

2004

Volltextzugriff (PDF)

Developmental differences in praxis in learning-disabled and normal children and adults

Perceptual and motor skills, 1994-06, Vol.78 (3 Pt 2), p.1219

1994

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The mechanisms for adult-onset apraxia and developmental dyspraxia: an examination and comparison of error patterns

The American journal of occupational therapy, 1997-05, Vol.51 (5), p.339-346

1997

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

American journal of hematology, 1993-08, Vol.43 (4), p.246-250

1993

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Pattern of 6-mercaptopurine urinary excretion in children with acute lymphoblastic leukemia : urinary assays as a measure of drug compliance

Therapeutic drug monitoring, 1992-10, Vol.14 (5), p.371-375

1992

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

Leukemia research, 1992-12, Vol.16 (12), p.1197-1201

1992

Volltextzugriff (PDF)

Comparative study of fanconi anemia in children of different ethnic origin in South Africa

American journal of medical genetics, 1994-09, Vol.52 (3), p.279-284

1994

Volltextzugriff (PDF)

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"I'm still dad": The Impact of Scleroderma on being a Father

Parenting: the forgotten role of women living with systemic lupus erythematosus

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

Measuring Dexterity in Children Using the Nine-hole Peg Test

Occupation of motherhood: challenges for mothers with scleroderma

Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

Perceived Parenting Ability and Systemic Sclerosis

Effect of Wrist Hand Splints on Grip, Pinch, Manual Dexterity, and Muscle Activation in Children with Spastic Hemiplegia: A Preliminary Study

Paediatric cancer survivors demonstrate a high rate of subclinical renal dysfunction

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

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

Micafungin Versus Liposomal Amphotericin B for Pediatric Patients With Invasive Candidiasis: Substudy of a Randomized Double-Blind Trial

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

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

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

Malignancies in South African children with HIV

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

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

Hepatocellular carcinoma and liver tumors in South African children: A case for increased prevalence

Developmental differences in praxis in learning-disabled and normal children and adults

The mechanisms for adult-onset apraxia and developmental dyspraxia: an examination and comparison of error patterns

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

Pattern of 6-mercaptopurine urinary excretion in children with acute lymphoblastic leukemia : urinary assays as a measure of drug compliance

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

Comparative study of fanconi anemia in children of different ethnic origin in South Africa

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