Hydrops fetalis in four siblings caused by galactosialidosis

A reference model of circulating hematopoietic stem cells across the lifespan with applications to diagnostics.

Nature medicine·2025

A multichannel feature-based approach for longitudinal lung CT registration in the presence of radiation induced lung damage.

Physics in medicine and biology·2021

In Silico Ventilation Within the Dose-Volume is Predictive of Lung Function Post-radiation Therapy in Patients with Lung Cancer.

Annals of biomedical engineering·2020

Prediction of a positive circumferential resection margin at surgery following neoadjuvant chemotherapy for adenocarcinoma of the oesophagus.

BJS open·2019

Elective cesarean delivery at term and the long-term risk for endocrine and metabolic morbidity of the offspring.

Journal of developmental origins of health and disease·2018

Impact of incremental circumferential resection margin distance on overall survival and recurrence in oesophageal adenocarcinoma.

BJS open·2018

Electroencephalography in the evaluation of headache patients: a review.

Israel journal of medical sciences·1998

Complementary medicine--a critical review.

Israel journal of medical sciences·1998

The Israel Longitudinal Mortality Study--differential mortality in Israel 1983-1992: objectives, materials, methods and preliminary results.

Israel journal of medical sciences·1998

Detection and typing of human papillomavirus DNAs by restriction endonuclease mapping of the PCR products.

Israel journal of medical sciences·1998

A comparison between arterial- and venous-sampled activated clotting time measurements.

Israel journal of medical sciences·1998

Heart rate variability in patients with secondary amyloidosis.

Israel journal of medical sciences·1998

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

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Hydrops fetalis in four siblings caused by galactosialidosis

Related Concept Videos

A reference model of circulating hematopoietic stem cells across the lifespan with applications to diagnostics.

A multichannel feature-based approach for longitudinal lung CT registration in the presence of radiation induced lung damage.

In Silico Ventilation Within the Dose-Volume is Predictive of Lung Function Post-radiation Therapy in Patients with Lung Cancer.

Prediction of a positive circumferential resection margin at surgery following neoadjuvant chemotherapy for adenocarcinoma of the oesophagus.

Elective cesarean delivery at term and the long-term risk for endocrine and metabolic morbidity of the offspring.

Impact of incremental circumferential resection margin distance on overall survival and recurrence in oesophageal adenocarcinoma.

Electroencephalography in the evaluation of headache patients: a review.

Complementary medicine--a critical review.

The Israel Longitudinal Mortality Study--differential mortality in Israel 1983-1992: objectives, materials, methods and preliminary results.

Detection and typing of human papillomavirus DNAs by restriction endonuclease mapping of the PCR products.

A comparison between arterial- and venous-sampled activated clotting time measurements.

Heart rate variability in patients with secondary amyloidosis.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Related Experiment Videos

Hydrops fetalis in four siblings caused by galactosialidosis

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