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Publications by Jun Ino
PKD1 Mutation May Epistatically Ameliorate Nephronophthisis Progression in Patients With NPHP1 Deletion
Clinical Case Reports
Medicine
Related publications
NPHP1 Gene Deletion Is a Rare Cause of Joubert Syndrome Related Disorders
Journal of Medical Genetics
Genetics
A Deletion in Nephronophthisis 4 (NPHP4) Is Associated With Recessive Cone-Rod Dystrophy in Standard Wire-Haired Dachshund
Genome Research
Genetics
Nephronophthisis
European Journal of Human Genetics
Genetics
How Ameliorate the Adherence in Patients With Inflammatory Bowel Disease?
Scandinavian Journal of Gastroenterology
Gastroenterology
Somatic Point Mutation of the Wild-Type Allele Detected in Tumors of Patients With VHL Germline Deletion
Oncogene
Cancer Research
Genetics
Molecular Biology
Progression of Coronary Calcium Burden and Carotid Stiffness in Patients With Essential Thrombocythemia Associated With JAK2 V617F Mutation
Atherosclerosis
Cardiovascular Medicine
Cardiology
Nephronophthisis
Pediatric Nephrology
Child Health
Pediatrics
Perinatology
Nephrology
Chemoimmunotherapy May Overcome the Adverse Prognostic Significance of 11q Deletion in Previously Untreated Patients With Chronic Lymphocytic Leukemia
Cancer
Cancer Research
Oncology
P3.16-35 Stair Climbing Exercise May Ameliorate Pulmonary Function Impairment in Patients at One Month After Lung Cancer Resection
Journal of Thoracic Oncology
Medicine
Oncology
Respiratory Medicine
Pulmonary
