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The Prognostic Association of Prostate MRI PI-RADS™ v2 Assessment Category and Risk of Biochemical Recurrence after Definitive Local Therapy for Prostate Cancer: A Systematic Review and Meta-Analysis

The Journal of urology, 2021-09, Vol.206 (3), p.507-516

2021

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The Sobriety Treatment and Recovery Teams program for families with parental substance use: Comparison of child welfare outcomes through 12 months post-intervention

Child abuse & neglect, 2021-10, Vol.120, p.105260-105260, Article 105260

2021

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Molecular characterisation of congenital myasthenic syndromes in Southern Brazil

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81 (9), p.973-977

2010

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Changes in differential gene expression in fibroblast cells from patients with triple A syndrome under oxidative stress

Hormone and metabolic research, 2013-02, Vol.45 (2), p.102-108

2013

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Sobriety Treatment and Recovery Teams for families with co-occurring substance use and child maltreatment: A randomized controlled trial

Child abuse & neglect, 2021-04, Vol.114, p.104963-104963, Article 104963

2021

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Differences in mutations across tumour sizes in clear-cell renal cell carcinoma

BJU international, 2024-09

2024

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Clinical parameters for the prediction of occult lymph node metastasis in patients with negative PSMA-PET

Urologic oncology, 2024-04, Vol.42 (4), p.115.e9-115.e16

2024

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Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management

Endocrine reviews, 2022-02, Vol.43 (1), p.91-159

2022

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Triple A syndrome: genotype-phenotype assessment

Clinical genetics, 2003-05, Vol.63 (5), p.415-417

2003

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Medication-Assisted Treatment Improves Child Permanency Outcomes for Opioid-Using Families in the Child Welfare System

Journal of substance abuse treatment, 2016-12, Vol.71, p.63-67

2016

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Identifying Homogeneous Outcome Groups in Adult Rehabilitation Using Cluster Analysis

The American journal of occupational therapy, 2019-09, Vol.73 (5), p.7305205050p1-7305205050p9

2019

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Focal high‐intensity focused ultrasound therapy for localized prostate cancer: An interim analysis of the multinational FASST study

European journal of clinical investigation, 2024-06, Vol.54 (6), p.e14192-n/a

2024

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Pathology of inherited manganese transporter deficiency

Annals of neurology, 2014-04, Vol.75 (4), p.608-612

2014

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The role of taxane-based chemotherapy in the treatment of prostate cancer

Current opinion in urology, 2020-07, Vol.30 (4), p.527-533

2020

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Peer mentoring services, opportunities, and outcomes for child welfare families with substance use disorders

Children and youth services review, 2018-01, Vol.84, p.239-246

2018

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Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients

Neurology, 2003-06, Vol.60 (11), p.1805-1810

2003

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Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

Brain (London, England : 1878), 2014-03, Vol.137 (Pt 3), p.683-692

2014

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Analysis of Microarray-based Gene Expression Datasets of Gliomas for the Identification of Potential Prognostic Markers and Unknown Signaling Pathways

International journal of radiation oncology, biology, physics, 2010, Vol.78 (3), p.S493-S493

2010

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Journal of medical genetics, 2004-11, Vol.41 (11), p.842-848

2004

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Laminated turbo codes: A new class of block-convolutional codes

IEEE transactions on information theory, 2008-07, Vol.54 (7), p.3024-3034

2008

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Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception

PLoS genetics, 2016-12, Vol.12 (12), p.e1006461-e1006461

2016

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Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

Nature genetics, 2011-02, Vol.43 (2), p.132-137

2011

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Sobriety treatment and recovery teams for families with co-occurring substance use and child maltreatment: A propensity score-matched evaluation

Children and youth services review, 2021-12, Vol.131, p.106256, Article 106256

2021

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Psycho-organic symptoms as early manifestation of adult onset POMT1 -related limb girdle muscular dystrophy

Neuromuscular disorders : NMD, 2014-11, Vol.24 (11), p.990-992

2014

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Double Serially Concatenated Convolutional Codes With Jointly Designed S-Type Permutors

IEEE transactions on information theory, 2009-12, Vol.55 (12), p.5811-5821

2009

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The Prognostic Association of Prostate MRI PI-RADS™ v2 Assessment Category and Risk of Biochemical Recurrence after Definitive Local Therapy for Prostate Cancer: A Systematic Review and Meta-Analysis

The Sobriety Treatment and Recovery Teams program for families with parental substance use: Comparison of child welfare outcomes through 12 months post-intervention

Molecular characterisation of congenital myasthenic syndromes in Southern Brazil

Changes in differential gene expression in fibroblast cells from patients with triple A syndrome under oxidative stress

Sobriety Treatment and Recovery Teams for families with co-occurring substance use and child maltreatment: A randomized controlled trial

Differences in mutations across tumour sizes in clear-cell renal cell carcinoma

Clinical parameters for the prediction of occult lymph node metastasis in patients with negative PSMA-PET

Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management

Triple A syndrome: genotype-phenotype assessment

Medication-Assisted Treatment Improves Child Permanency Outcomes for Opioid-Using Families in the Child Welfare System

Identifying Homogeneous Outcome Groups in Adult Rehabilitation Using Cluster Analysis

Focal high‐intensity focused ultrasound therapy for localized prostate cancer: An interim analysis of the multinational FASST study

Pathology of inherited manganese transporter deficiency

The role of taxane-based chemotherapy in the treatment of prostate cancer

Peer mentoring services, opportunities, and outcomes for child welfare families with substance use disorders

Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

Analysis of Microarray-based Gene Expression Datasets of Gliomas for the Identification of Potential Prognostic Markers and Unknown Signaling Pathways

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Laminated turbo codes: A new class of block-convolutional codes

Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception

Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

Sobriety treatment and recovery teams for families with co-occurring substance use and child maltreatment: A propensity score-matched evaluation

Psycho-organic symptoms as early manifestation of adult onset POMT1 -related limb girdle muscular dystrophy

Double Serially Concatenated Convolutional Codes With Jointly Designed S-Type Permutors

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