Mike Fitzpatrick

Dr. Mike Fitzpatrick

Independent Researcher and Consultant
orcid

Research Focus & Metrics

Academic Career Length

103Years (1924-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 1998 in Experimental Biology and Medicine
Verified
Journal Article
Open access
CIC. H. G. Irvine
C. H. G. Irvine
MFMike Fitzpatrick
Mike Fitzpatrick
SAS. L. Alexander
S. L. Alexander
Exposure to estrogenic compounds may pose a developmental hazard to infants. Soy products, which contain the phytoestrogens, genistein and daidzein, are becoming increasingly popular as inf...

1 December 1998 in The American Journal of Clinical Nutrition
Verified
Journal Article
Open access
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CIClifford Hg Irvine
Clifford Hg Irvine
NSNatalie Shand
Natalie Shand
MFMike Fitzpatrick
Mike Fitzpatrick
SASusan L Alexander
Susan L Alexander
Our aims were to measure isoflavone intake from soy- and dairy-based infant formulas and breast milk and to assess the ability of infants to digest and absorb soy isoflavones by measuring daily urinary excretion rates. We recruited 29 infants: 4 received soy-based formula and 25 received dairy-based formula. We collected pooled urine samples from 3-5 disposable diapers worn during a 24-h period and developed and validated methods for extracting isoflavones from the diapers. Infants were studied every 1 or 2 wk, starting at 2-6 wk of age and continuing until 16 wk. Only soy-based formulas contained isoflavones in concentrations detectable by HPLC (limits: 0.05 mg/L for liquids and 0.1 mg/kg for solids). Soy-based formulas provided a mean (+/-SEM) daily dose of isoflavones (genistein plus daidzein) of 3.2 +/- 0.2 mg/kg body wt, which remained fairly constant (CV: 12%) regardless of age < or = 16 wk. Isoflavones were measurable in all samples from soy-fed infants, but not in urine from dairy-fed infants. Daily isoflavone excretion rates varied little among infants [range of mean individual values (mg x kg(-1) d(-1)): daidzein, 0.37 +/- 0.03 to 0.58 +/- 0.06; genistein, 0.15 +/- 0.03 to 0.32 +/- 0.04] and did not change with age < or = 16 wk. The mean percentage of the daily intake recovered in the urine of soy-fed infants was 38 +/- 4% for daidzein and 13 +/- 3% for genistein, and remained constant with age. These values are similar to those for adults and indicate that young infants are able to digest, absorb, and excrete genistein and daidzein from soy-based formulas as efficiently as do adults consuming soy products.

16 July 2018 in Antioxidants
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Journal Article
Open access
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MFMike N. Foster
Mike N. Foster
Anitra CarrAnitra Carr
Anitra Carr
AAAlina Antony
Alina Antony
SPSelene Peng
Selene Peng
MFMike Fitzpatrick
Mike Fitzpatrick
A 52-year-old female presented to Integrated Health Options Clinic in October 2014 with a history of relapsed acute myeloid leukaemia (AML, diagnosed in 2009 and relapsed in 2014). Intravenous(IV) vitamin C therapy was initiated (in 2014) following completion of chemotherapy as an alternative to haematopoietic stem cell transplantation. IV vitamin C was administered twice weekly at a dose of 70 g/infusion. Within 4 weeks of initiation of IV vitamin C therapy, there was a dramatic improvement in the patient’s blood indices with platelet cell counts increasing from 25 × 109/L to 196 × 109/L and white blood cell counts increasing from 0.29 × 109/L to 4.0 × 109/L, with further improvements observed over the next 18 months. Furthermore, there was a clear and sustained improvement in the patient’s health-related quality of life scores assessed using a validated questionnaire. She has remained healthy and in complete remission until the present day. This case study highlights the benefits of IV vitamin C as a supportive therapy for previously relapsed AML.

1 October 1998 in Inorganica Chimica Acta
Verified
Journal Article
Closed access
MFMike Fitzpatrick
Mike Fitzpatrick
LHLyall R. Hanton
Lyall R. Hanton
WHWilliam Henderson
William Henderson
PKPenelope E. Kneebone
Penelope E. Kneebone
ELEsther G. Levy
Esther G. Levy
DMDavid A. McMorran
David A. McMorran

9 March 2020 in Genealogy
Verified
Journal Article
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Esther FitzpatrickEsther Fitzpatrick
Esther Fitzpatrick
MFMike Fitzpatrick
Mike Fitzpatrick
DNA analysis has enabled a much deeper interrogation of our surnames, Keesing and Fitzpatrick, than was possible via traditional genealogical research. This can inform us regarding the potential ‘hidden’ complexities of some surnames. Through juxtaposing the narratives of our family histories and DNA findings we demonstrate, using collaborative autoethnography, how surnames can be haunted by ghosts both real and imagined. The DNA-enabled critical exploration of the history of our surnames, in the context of the social and political factors that shaped them, generates a deeper and more complex understanding of how our surnames were taken/given. In this paper we investigate and deconstruct our Irish and Jewish ancestry. Fitzpatrick and Keesing are anglicised/normanised/colonised surnames that exemplify attempts to dis/member our identities. Here we re/member them, but with that comes a realisation that ‘everything has changed’ and with that come new dis/memberings and re/memberings.