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Advanced hepatocellular carcinoma with MET-amplified contained excellent response to crizotinib: a case report

Frontiers in oncology, 2023, Vol.13, p.1196211-1196211

2023

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Case Report: A Novel Homozygous Mutation of Cyclin O Gene Mutation in Primary Ciliary Dyskinesia with Short Stature

Pharmacogenomics and personalized medicine, 2023, Vol.16, p.443-448

2023

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Upper gastrointestinal tract immune-related adverse events: Two cases of obstructive complications occurred in immune consolidation therapy after sequential chimeric antigen receptor T cell therapy with autologous hematopoietic stem cell transplantation for refractory/relapsed diffuse large B cell lymphoma

Clinical case reports, 2024, Vol.12 (1), p.e8411-e8411

2024

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A Case of Floating-Harbor Syndrome with "Growth and Language Development Delay" as Its Clinical Manifestation

Pharmacogenomics and personalized medicine, 2023, Vol.16, p.1091-1096

2023

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A Case Report of Cardiofaciocutaneous Syndrome with MAP2K1 Pathogenic Variant

Pharmacogenomics and personalized medicine, 2023, Vol.16, p.817-823

2023

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Myotonic dystrophy type 1 presenting with dyspnea: A case report

World journal of clinical cases, 2022, Vol.10 (20), p.7060-7067

2022

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Osteoblastoma of the breast:An uncommon and easily overlooked location

Radiology case reports, 2021, Vol.16 (7), p.1633-1636

2021

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Multimodality imaging in diagnosing lipomatous atrial septal hypertrophy with atrial septal defect: a case report

Frontiers in cardiovascular medicine, 2023, Vol.10, p.1245213-1245213

2023

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Fire acupuncture for anti-LGI1 antibody autoimmune encephalitis: a case report

Frontiers in neuroscience, 2023, Vol.17, p.1203915-1203915

2023

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One-stage revision arthroplasty in a patient with ochronotic arthropathy accompanied by joint infection: A case report

World journal of clinical cases, 2022, Vol.10 (25), p.9036-9043

2022

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Foreign accent syndrome following herpes simplex encephalitis: a case report

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020, Vol.41 (9), p.2643-2645

2020

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Clinical and genetic features of Epstein-Barr virus-triggered late-onset primary hemophagocytic lymphohistiocytosis: Ten pedigrees study

Clinical and translational medicine, 2021, Vol.11 (6), p.e393-e393

2021

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Sequential CAR T-Cell Therapy After Autologous Stem Cell Transplantation for the Treatment of Relapsed/Refractory Intravascular Large B-Cell Lymphoma With Central Nervous System Involvement: A Case Report

Frontiers in oncology, 2022, Vol.12, p.817969-817969

2022

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Case Report: Chronic Lymphocytic Leukemia With a Rare Translocation t(14;19)(q32;q13) Involving IGH/BCL3 Rearrangements: Report of Three Chinese Cases and Literature Review

Frontiers in oncology, 2020, Vol.10, p.594732-594732

2020

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Chronic myelomonocytic leukemia with double-mutations in DNMT3A and FLT3-ITD treated with decitabine and sorafenib

Cancer Biology & Therapy, 2017, Vol.18 (11), p.843-849

2017

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A Novel e8a2BCR-ABL1 Fusion Transcript without Insertion Sequence in a Patient with Chronic Myeloid Leukemia

Annals of laboratory medicine, 2018, Vol.38 (2), p.169-171

2018

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Homozygous PIGT Mutation Lead to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3

Frontiers in genetics, 2018, Vol.9, p.153-153

2018

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A novel e8a2 BCR-ABL1 intronic fusion through insertion of a chromosome 22 BCR gene fragment into chromosome 9 in an atypical Philadelphia (Ph) chromosome chronic myeloid leukemia patient

Leukemia & lymphoma, 2016, Vol.57 (12), p.2930-2933

2016

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Automated Peritoneal Dialysis is Suitable for Polycystic Kidney Disease Patients with End-Stage Renal Disease

Case reports in nephrology and dialysis, 2015, Vol.5 (2), p.140-144

2015

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Hidradenitis suppurativa associated with a novel NCSTN mutation and concomitant Klippel-Trenaunay syndrome

European journal of dermatology : EJD, 2021, Vol.31 (2), p.246-248

2021

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Papular acantholytic dyskeratosis of the anogenital area with novel ATP2C1 gene mutations

Chinese medical journal, 2021, Vol.134 (12), p.1508-1510

2021

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Hemoporfin photodynamic therapy for a case of unilateral nevoid telangiectasia

Chinese medical journal, 2020, Vol.134 (10), p.1245-1247

2020

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Reversible cardiogenic shock caused by atrioventricular junctional rhythm after percutaneous coronary intervention

Journal of geriatric cardiology : JGC, 2012, Vol.9 (3), p.318-320

2012

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A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling

Therapeutics and clinical risk management, 2015, Vol.11, p.635-638

2015

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Advanced hepatocellular carcinoma with MET-amplified contained excellent response to crizotinib: a case report

Case Report: A Novel Homozygous Mutation of Cyclin O Gene Mutation in Primary Ciliary Dyskinesia with Short Stature

A Case of Floating-Harbor Syndrome with "Growth and Language Development Delay" as Its Clinical Manifestation

A Case Report of Cardiofaciocutaneous Syndrome with MAP2K1 Pathogenic Variant

Myotonic dystrophy type 1 presenting with dyspnea: A case report

Osteoblastoma of the breast:An uncommon and easily overlooked location

Multimodality imaging in diagnosing lipomatous atrial septal hypertrophy with atrial septal defect: a case report

Fire acupuncture for anti-LGI1 antibody autoimmune encephalitis: a case report

One-stage revision arthroplasty in a patient with ochronotic arthropathy accompanied by joint infection: A case report

Foreign accent syndrome following herpes simplex encephalitis: a case report

Clinical and genetic features of Epstein-Barr virus-triggered late-onset primary hemophagocytic lymphohistiocytosis: Ten pedigrees study

Sequential CAR T-Cell Therapy After Autologous Stem Cell Transplantation for the Treatment of Relapsed/Refractory Intravascular Large B-Cell Lymphoma With Central Nervous System Involvement: A Case Report

Case Report: Chronic Lymphocytic Leukemia With a Rare Translocation t(14;19)(q32;q13) Involving IGH/BCL3 Rearrangements: Report of Three Chinese Cases and Literature Review

Chronic myelomonocytic leukemia with double-mutations in DNMT3A and FLT3-ITD treated with decitabine and sorafenib

A Novel e8a2BCR-ABL1 Fusion Transcript without Insertion Sequence in a Patient with Chronic Myeloid Leukemia

Homozygous PIGT Mutation Lead to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3

A novel e8a2 BCR-ABL1 intronic fusion through insertion of a chromosome 22 BCR gene fragment into chromosome 9 in an atypical Philadelphia (Ph) chromosome chronic myeloid leukemia patient

Automated Peritoneal Dialysis is Suitable for Polycystic Kidney Disease Patients with End-Stage Renal Disease

Hidradenitis suppurativa associated with a novel NCSTN mutation and concomitant Klippel-Trenaunay syndrome

Papular acantholytic dyskeratosis of the anogenital area with novel ATP2C1 gene mutations

Hemoporfin photodynamic therapy for a case of unilateral nevoid telangiectasia

Reversible cardiogenic shock caused by atrioventricular junctional rhythm after percutaneous coronary intervention

A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling

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