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Somatostatin analog therapy for severe polycystic liver disease: results after 2 years

Nephrology, dialysis, transplantation, 2012-09, Vol.27 (9), p.3532-3539

2012

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Frailty in patients over 65 years of age admitted to Intensive Care Units (FRAIL-ICU)

Medicina intensiva, 2019-10, Vol.43 (7), p.395-401

2019

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Family burden related to clinical and functional variables of people with intellectual disability with and without a mental disorder

Research in developmental disabilities, 2012-05, Vol.33 (3), p.796-803

2012

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Carbon Dioxide Laser Treatment in Hailey-Hailey Disease: A Series of 8 Patients

Actas dermo-sifiliográficas (English ed.), 2013-05, Vol.104 (4), p.325-333

2013

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Renal transplantation in antineutrophil cytoplasmic antibody-associated vasculitis: a multicenter experience

Transplantation, 2011-06, Vol.91 (12), p.1370

2011

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Clinical features of patients with immunoglobulin light chain amyloidosis (AL) with vascular-limited deposition in the kidney

Nephrology, dialysis, transplantation, 2012-03, Vol.27 (3), p.1097-1101

2012

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Efficacy of 4 Years of Octreotide Long-Acting Release Therapy in Patients With Severe Polycystic Liver Disease

Mayo Clinic proceedings, 2015-08, Vol.90 (8), p.1030-1037

2015

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Performance of the CKD-EPI Equation to Estimate GFR in a Longitudinal Study of Autosomal Dominant Polycystic Kidney Disease

American journal of kidney diseases, 2017-03, Vol.69 (3), p.482-484

2017

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Successful Pregnancy and Delivery of a Healthy Newborn Despite Transplacental Transfer of Antimyeloperoxidase Antibodies From a Mother With Microscopic Polyangiitis

American journal of kidney diseases, 2009-09, Vol.54 (3), p.542-545

2009

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Necrotic ulcerations on the back of the hands in a patient with chronic renal failure: An uncommon presentation of calciphylaxis

Journal of the American Academy of Dermatology, 2012-10, Vol.67 (4), p.e152-e154

2012

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Cavernous hemangiomas of the brain: report of 2 cases

Arquivos de neuro-psiquiatria, 1984-03, Vol.42 (1), p.32-40

1984

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Imaging classification of autosomal dominant polycystic kidney disease: a simple model for selecting patients for clinical trials

Journal of the American Society of Nephrology, 2015-01, Vol.26 (1), p.160-172

2015

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Outcomes and Durability of Hepatic Reduction after Combined Partial Hepatectomy and Cyst Fenestration for Massive Polycystic Liver Disease

Journal of the American College of Surgeons, 2016-07, Vol.223 (1), p.118-126.e1

2016

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Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2016-09, Vol.27 (9), p.2872-2884

2016

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Identification of Biomarkers for PKD1 Using Urinary Exosomes

Journal of the American Society of Nephrology, 2015-07, Vol.26 (7), p.1661-1670

2015

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Long-Term Administration of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease

Clinical journal of the American Society of Nephrology, 2018-08, Vol.13 (8), p.1153-1161

2018

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Effect of genotype on the severity and volume progression of polycystic liver disease in autosomal dominant polycystic kidney disease

Nephrology, dialysis, transplantation, 2016-06, Vol.31 (6), p.952-960

2016

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The regulatory 1α subunit of protein kinase A modulates renal cystogenesis

American journal of physiology. Renal physiology, 2017-09, Vol.313 (3), p.F677-F686

2017

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Newborn screening for homocystinurias: Recent recommendations versus current practice

Journal of inherited metabolic disease, 2019-01, Vol.42 (1), p.128-139

2019

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Presymptomatic Screening for Intracranial Aneurysms in Patients with Autosomal Dominant Polycystic Kidney Disease

Clinical journal of the American Society of Nephrology, 2019-08, Vol.14 (8), p.1151-1160

2019

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Volume regression of native polycystic kidneys after renal transplantation

Nephrology, dialysis, transplantation, 2016-01, Vol.31 (1), p.73-79

2016

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Urinary Albumin Excretion Patterns of Patients with Cast Nephropathy and Other Monoclonal Gammopathy–Related Kidney Diseases

Clinical journal of the American Society of Nephrology, 2012-12, Vol.7 (12), p.1964-1968

2012

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Congenital Heart Disease in Adults with Autosomal Dominant Polycystic Kidney Disease

American journal of nephrology, 2022-05, Vol.53 (4), p.316-324

2022

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Isthmin-1 (ISM1), a novel adipokine that reflects abdominal adipose tissue distribution in individuals with obesity

Cardiovascular diabetology, 2023-12, Vol.22 (1), p.335-335, Article 335

2023

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Amino Acid Profile in Malnourished Patients with Liver Cirrhosis and Its Modification with Oral Nutritional Supplements: Implications on Minimal Hepatic Encephalopathy

Nutrients, 2021-10, Vol.13 (11), p.3764

2021

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Somatostatin analog therapy for severe polycystic liver disease: results after 2 years

Frailty in patients over 65 years of age admitted to Intensive Care Units (FRAIL-ICU)

Family burden related to clinical and functional variables of people with intellectual disability with and without a mental disorder

Carbon Dioxide Laser Treatment in Hailey-Hailey Disease: A Series of 8 Patients

Renal transplantation in antineutrophil cytoplasmic antibody-associated vasculitis: a multicenter experience

Clinical features of patients with immunoglobulin light chain amyloidosis (AL) with vascular-limited deposition in the kidney

Efficacy of 4 Years of Octreotide Long-Acting Release Therapy in Patients With Severe Polycystic Liver Disease

Performance of the CKD-EPI Equation to Estimate GFR in a Longitudinal Study of Autosomal Dominant Polycystic Kidney Disease

Successful Pregnancy and Delivery of a Healthy Newborn Despite Transplacental Transfer of Antimyeloperoxidase Antibodies From a Mother With Microscopic Polyangiitis

Necrotic ulcerations on the back of the hands in a patient with chronic renal failure: An uncommon presentation of calciphylaxis

Cavernous hemangiomas of the brain: report of 2 cases

Imaging classification of autosomal dominant polycystic kidney disease: a simple model for selecting patients for clinical trials

Outcomes and Durability of Hepatic Reduction after Combined Partial Hepatectomy and Cyst Fenestration for Massive Polycystic Liver Disease

Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney Disease

Identification of Biomarkers for PKD1 Using Urinary Exosomes

Long-Term Administration of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease

Effect of genotype on the severity and volume progression of polycystic liver disease in autosomal dominant polycystic kidney disease

The regulatory 1α subunit of protein kinase A modulates renal cystogenesis

Newborn screening for homocystinurias: Recent recommendations versus current practice

Presymptomatic Screening for Intracranial Aneurysms in Patients with Autosomal Dominant Polycystic Kidney Disease

Volume regression of native polycystic kidneys after renal transplantation

Urinary Albumin Excretion Patterns of Patients with Cast Nephropathy and Other Monoclonal Gammopathy–Related Kidney Diseases

Congenital Heart Disease in Adults with Autosomal Dominant Polycystic Kidney Disease

Isthmin-1 (ISM1), a novel adipokine that reflects abdominal adipose tissue distribution in individuals with obesity

Amino Acid Profile in Malnourished Patients with Liver Cirrhosis and Its Modification with Oral Nutritional Supplements: Implications on Minimal Hepatic Encephalopathy

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