[X-linked familial pituitary nanism]

Germline heterozygous SH2B3 p.Glu78Lys variant: a three-patient case series with myeloproliferative neoplasms.

Experimental hematology·2025

Synergistic use of bioactive agents for the management of different skin conditions: an overview of biological activities.

European review for medical and pharmacological sciences·2023

Severe Bartter syndrome type 1: Prompt postnatal management thanks to antenatal identification of SLC12A1 pathogenic variants.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2022

Genome-wide analyses reveal the regions involved in the phenotypic diversity in Sicilian pigs.

Animal genetics·2019

Correction to: Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres.

Annals of hematology·2018

Tissue factor (:Factor VIIa) in the heart and vasculature: More than an envelope.

Thrombosis research·2018

Breast carcinoma metastasizing to an adrenocortical adenoma: a case of tumour-to-tumour metastasis.

Pathologica·2026

Metastatic melanoma with heterologous bone after neoadjuvant immunotherapy: diagnostic insights.

Pathologica·2026

Lymphangitic breast cancer in explanted lungs with interstitial lung disease: an unexpected finding.

Pathologica·2026

Histological insights into sudden, unexpected death due to tuberculosis: two autopsy case reports and review of the literature.

Pathologica·2026

Teaching with human remains: curatorship, technological innovation and ethical engagement at the Morgagni Museum of Human Anatomy.

Pathologica·2026

Technical feasibility of a long read, fourth generation sequencing platform in diagnostic profiling of clinical routine samples: a proof-of-concept study.

Pathologica·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

GBA1 variants and mortality in Parkinson's disease: A systematic review and meta-analysis.

Journal of Parkinson's disease·2026

[Associations of candidate gene polymorphisms, gut microbiota, and their interactions with NAFLD in obese children].

Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences·2026

Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.

Annals of the Child Neurology Society·2026

Lesions Associated With Autism Symptoms Map to a Cerebellar Brain Network in Tuberous Sclerosis Complex.

Annals of the Child Neurology Society·2026

Hemimegalencephaly and intractable focal seizures related to NPRL3 mutation with variable familial expressivity treated with anatomic hemispherectomy.

Annals of the Child Neurology Society·2026

Related Experiment Videos

[X-linked familial pituitary nanism]

Related Concept Videos

Germline heterozygous SH2B3 p.Glu78Lys variant: a three-patient case series with myeloproliferative neoplasms.

Synergistic use of bioactive agents for the management of different skin conditions: an overview of biological activities.

Severe Bartter syndrome type 1: Prompt postnatal management thanks to antenatal identification of SLC12A1 pathogenic variants.

Genome-wide analyses reveal the regions involved in the phenotypic diversity in Sicilian pigs.

Correction to: Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres.

Tissue factor (:Factor VIIa) in the heart and vasculature: More than an envelope.

Breast carcinoma metastasizing to an adrenocortical adenoma: a case of tumour-to-tumour metastasis.

Metastatic melanoma with heterologous bone after neoadjuvant immunotherapy: diagnostic insights.

Lymphangitic breast cancer in explanted lungs with interstitial lung disease: an unexpected finding.

Histological insights into sudden, unexpected death due to tuberculosis: two autopsy case reports and review of the literature.

Teaching with human remains: curatorship, technological innovation and ethical engagement at the Morgagni Museum of Human Anatomy.

Technical feasibility of a long read, fourth generation sequencing platform in diagnostic profiling of clinical routine samples: a proof-of-concept study.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

GBA1 variants and mortality in Parkinson's disease: A systematic review and meta-analysis.

[Associations of candidate gene polymorphisms, gut microbiota, and their interactions with NAFLD in obese children].

Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.

Lesions Associated With Autism Symptoms Map to a Cerebellar Brain Network in Tuberous Sclerosis Complex.

Hemimegalencephaly and intractable focal seizures related to NPRL3 mutation with variable familial expressivity treated with anatomic hemispherectomy.

Related Experiment Videos

[X-linked familial pituitary nanism]

Related Concept Videos

Related Articles