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Scalpellum occulta: A rare case of dorsal spinal arachnoid web without the scalpel sign

Radiology case reports, 2024-04, Vol.19 (4), p.1552-1555

2024

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Concurrence of chromosome 6 chromothripsis and glioblastoma metastasis

Journal of neurosurgery, 2017-05, Vol.126 (5), p.1472-1478

2017

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Basal impulses: findings from the last twenty years on impulsivity and reward pathways using deep brain stimulation

Journal of neurosurgical sciences, 2020-12, Vol.64 (6)

2020

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Electric motor do's and don'ts

Energy engineering, 1994, Vol.91 (1), p.6-24

HOSHIDE, R. K

1994

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Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis

Journal of inherited metabolic disease, 1993-01, Vol.16 (1), p.31-38

1993

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Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency

Journal of inherited metabolic disease, 1995-05, Vol.18 (3), p.273-282

1995

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Specificity of PCR‐SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency

Journal of inherited metabolic disease, 1993-09, Vol.16 (5), p.857-862

1993

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Emergence of community-acquired extended-spectrum beta-lactamase Escherichia coli (ESBLEC) in Honolulu: a case series of three individuals with community-acquired ESBLEC bacteriuria

Hawaii medical journal (1962), 2011-09, Vol.70 (9), p.193

2011

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Effective energy audits

Energy engineering, 1995-01, Vol.92 (6), p.6-17

HOSHIDE, R. K

1995

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The polymorphic 43Thr bcl-2 protein confers relative resistance to autoimmunity : an analytical evaluation

Human genetics, 1998-10, Vol.103 (4), p.435-440

1998

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Barriers to healthcare of homeless residents of three Honolulu shelters

Hawaii medical journal (1962), 2011-10, Vol.70 (10), p.214

2011

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Molecular basis of urea cycle disorders

Nihon rinshō, 1993-02, Vol.51 (2), p.520

1993

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Molecular Cloning, Tissue Distribution, and Chromosomal Localization of Human Cationic Amino Acid Transporter 2 (HCAT2)

Genomics (San Diego, Calif.), 1996-12, Vol.38 (2), p.174-178

1996

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Favorable outcomes for Native Hawaiians and other Pacific Islanders with severe traumatic brain injury

Hawai'i journal of medicine & public health, 2013-04, Vol.72 (4), p.129-135

2013

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Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency

Human mutation, 1998, Vol.11 (S1), p.S5-S7

1998

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Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adult

Journal of medical genetics, 1996-08, Vol.33 (8), p.645-648

1996

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For novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency : application of PCR-single-strand conformation polymorphisms for all exons and adjacent introns

Human genetics, 1993-08, Vol.92 (1), p.49-56

1993

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The R40h mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients

Human genetics, 1997-02, Vol.99 (2), p.171-176

1997

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Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male

Human mutation, 1998, Vol.11 (S1), p.S131-S133

1998

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Carbamyl phosphate synthetase I deficiency : one base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicing

The Journal of clinical investigation, 1993-05, Vol.91 (5), p.1884-1887

1993

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Scalpellum occulta: A rare case of dorsal spinal arachnoid web without the scalpel sign

Radiology case reports, 2024, Vol.19 (4), p.1552-1555

2024

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Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male

Human mutation, 1998, Vol.Suppl 1, p.S131-S133

1998

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Energy Conservation Measures (ECMs): Which Projects Should We Select?

Strategic planning for energy and the environment, 1999, Vol.18 (3), p.43-51

Hoshide, Robert K.

1999

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Carbamyl phosphate synthetase I deficiency

Ryoikibetsu shokogun shirizu, 1998 (18 Pt 1), p.167

Hoshide, R

1998

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Assignment of the Human Carbamyl Phosphate Synthetase I Gene (CPS1) to 2q35 by Fluorescence in Situ Hybridization

Genomics (San Diego, Calif.), 1995-07, Vol.28 (1), p.124-125

1995

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Scalpellum occulta: A rare case of dorsal spinal arachnoid web without the scalpel sign

Concurrence of chromosome 6 chromothripsis and glioblastoma metastasis

Basal impulses: findings from the last twenty years on impulsivity and reward pathways using deep brain stimulation

Electric motor do's and don'ts

Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis

Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency

Specificity of PCR‐SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency

Emergence of community-acquired extended-spectrum beta-lactamase Escherichia coli (ESBLEC) in Honolulu: a case series of three individuals with community-acquired ESBLEC bacteriuria

Effective energy audits

The polymorphic 43Thr bcl-2 protein confers relative resistance to autoimmunity : an analytical evaluation

Barriers to healthcare of homeless residents of three Honolulu shelters

Molecular basis of urea cycle disorders

Molecular Cloning, Tissue Distribution, and Chromosomal Localization of Human Cationic Amino Acid Transporter 2 (HCAT2)

Favorable outcomes for Native Hawaiians and other Pacific Islanders with severe traumatic brain injury

Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency

Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adult

For novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency : application of PCR-single-strand conformation polymorphisms for all exons and adjacent introns

The R40h mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients

Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male

Carbamyl phosphate synthetase I deficiency : one base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicing

Scalpellum occulta: A rare case of dorsal spinal arachnoid web without the scalpel sign

Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male

Energy Conservation Measures (ECMs): Which Projects Should We Select?

Carbamyl phosphate synthetase I deficiency

Assignment of the Human Carbamyl Phosphate Synthetase I Gene (CPS1) to 2q35 by Fluorescence in Situ Hybridization

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