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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

Human molecular genetics, 2000, Vol.9 (1), p.27-34

2000

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Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

Nature genetics, 1997-10, Vol.17 (2), p.198-200

1997

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Diagnostic Accuracy of Point-of-Care Lung Ultrasonography and Chest Radiography in Adults With Symptoms Suggestive of Acute Decompensated Heart Failure: A Systematic Review and Meta-analysis

JAMA network open, 2019-03, Vol.2 (3), p.e190703-e190703

2019

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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

Nature (London), 1993-04, Vol.362 (6422), p.749-751

1993

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Implications of Guideline Updates for the Management of Apparent Treatment Resistant Hypertension in the United States (A NCDR Research to Practice [R2P] Project)

The American journal of cardiology, 2020-01, Vol.125 (1), p.63-67

2020

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Longitudinal Analysis of Serological Responses of Adults to Helicobacter pylori Antigens

The Journal of infectious diseases, 2010-09, Vol.202 (6), p.916-923

2010

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Effects of 8 weeks of CPAP on lipid‐based oxidative markers in obstructive sleep apnea: a randomized trial

Journal of sleep research, 2015-06, Vol.24 (3), p.339-345

2015

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Impact of a Palliative Care Program on Tracheostomy Utilization in a Community Hospital

Journal of palliative medicine, 2015-12, Vol.18 (12), p.1070-1073

2015

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Language regression in childhood

Pediatric neurology, 2001-03, Vol.24 (3), p.183-189

2001

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Survival in patients with recurrent hepatocellular carcinoma after primary hepatectomy: Comparative effectiveness of treatment modalities

Surgery, 2012-05, Vol.151 (5), p.700-709

2012

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North American Paragonimiasis : A case report

Acta cytologica, 2000, Vol.44 (1), p.75-80

2000

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Connexin26 deafness in several interconnected families

Journal of medical genetics, 1999-05, Vol.36 (5), p.383-385

1999

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Oguchi disease: suggestion of linkage to markers on chromosome 2q

Journal of medical genetics, 1995-05, Vol.32 (5), p.396-398

1995

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The effect of periodic monitoring and feedback on screening colonoscopy withdrawal times, polyp detection rates, and patient satisfaction scores

Gastrointestinal endoscopy, 2010-06, Vol.71 (7), p.1253-1259

2010

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Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndrome

The Lancet (British edition), 1992-01, Vol.339 (8787), p.243-243

1992

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Patient satisfaction scores for endoscopic procedures: impact of a survey-collection method

Gastrointestinal endoscopy, 2007-05, Vol.65 (6), p.775-781

2007

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Positive nuclear expression of KLF8 might be correlated with shorter survival in gastric adenocarcinoma

Annals of diagnostic pathology, 2014-04, Vol.18 (2), p.74-77

2014

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Acute symptomatic small bowel obstruction due to capsule impaction

Gastrointestinal endoscopy, 2007-04, Vol.65 (4), p.725-728

2007

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Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2

Clinical & experimental ophthalmology, 2005-04, Vol.33 (2), p.129-136

2005

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Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness

American journal of medical genetics, 1998-01, Vol.75 (2), p.179-185

1998

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Portal-vein embolization after sclerotherapy treatment of bleeding gastric varices: report of a case with long-term follow-up

Gastrointestinal endoscopy, 2009-05, Vol.69 (6), p.1176-1178

2009

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Acute parotitis after double-balloon endoscopy

Gastrointestinal endoscopy, 2008-11, Vol.68 (5), p.1017-1019

2008

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Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination

Human mutation, 1998, Vol.11 (S1), p.S317-S319

1998

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Mitochondrial mutation associated with nonsyndromic deafness

American journal of otolaryngology, 1995-11, Vol.16 (6), p.403-408

1995

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A third Wilm's tumor locus on chromosome 16q

Cancer research (Chicago, Ill.), 1992-06, Vol.52 (11), p.3094-3098

1992

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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

Diagnostic Accuracy of Point-of-Care Lung Ultrasonography and Chest Radiography in Adults With Symptoms Suggestive of Acute Decompensated Heart Failure: A Systematic Review and Meta-analysis

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

Implications of Guideline Updates for the Management of Apparent Treatment Resistant Hypertension in the United States (A NCDR Research to Practice [R2P] Project)

Longitudinal Analysis of Serological Responses of Adults to Helicobacter pylori Antigens

Effects of 8 weeks of CPAP on lipid‐based oxidative markers in obstructive sleep apnea: a randomized trial

Impact of a Palliative Care Program on Tracheostomy Utilization in a Community Hospital

Language regression in childhood

Survival in patients with recurrent hepatocellular carcinoma after primary hepatectomy: Comparative effectiveness of treatment modalities

North American Paragonimiasis : A case report

Connexin26 deafness in several interconnected families

Oguchi disease: suggestion of linkage to markers on chromosome 2q

The effect of periodic monitoring and feedback on screening colonoscopy withdrawal times, polyp detection rates, and patient satisfaction scores

Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndrome

Patient satisfaction scores for endoscopic procedures: impact of a survey-collection method

Positive nuclear expression of KLF8 might be correlated with shorter survival in gastric adenocarcinoma

Acute symptomatic small bowel obstruction due to capsule impaction

Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2

Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness

Portal-vein embolization after sclerotherapy treatment of bleeding gastric varices: report of a case with long-term follow-up

Acute parotitis after double-balloon endoscopy

Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination

Mitochondrial mutation associated with nonsyndromic deafness

A third Wilm's tumor locus on chromosome 16q

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