Four examples of the S-s-U-phenotype in an Indian family

Developing and validating a new national remote health advice syndromic surveillance system in England.

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Outcomes research: contemporary issues and historical significance for nurse practitioners.

Journal of the American Academy of Nurse Practitioners·1996

Rh18 and hrS blood groups and antibodies.

Vox sanguinis·1994

STEM, a new low-frequency Rh antigen associated with the e-variant phenotypes hrS-(Rh: -18, -19) and hrB-(Rh: -31, -34).

Transfusion medicine (Oxford, England)·1993

Rh33 in two of three German siblings with D+ C+ c+ E- e+ red cells.

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Serology and genetics of the red blood cell factor Rh34.

Vox sanguinis·1991

Monitoring of lymphocyte subsets in regular blood donors.

Vox sanguinis·2026

Low-titer O whole-blood transfusion for life-threatening gastrointestinal and post-partum hemorrhage.

Vox sanguinis·2026

Rates of severe acute respiratory syndrome coronavirus 2 infection in a highly exposed South African blood donor cohort, 2022-2023.

Vox sanguinis·2026

Prospective multi-centre haemovigilance of amotosalen and ultraviolet A-treated platelets and plasma in routine clinical use.

Vox sanguinis·2026

Hemorrhagic shock in intensive care: Variation in blood product administration during resuscitation.

Vox sanguinis·2026

Right dose, right patient: Clinician-led implementation of a national cross-specialty strategy for immunoglobulin stewardship.

Vox sanguinis·2026

CLCN6 mutation in an Indian patient with rapidly progressive dementia.

Psychiatric genetics·2026

Neck vs Head Interspace Ratios in Hallux Valgus: A Reliability Analysis of First Metatarsal Radiographic Measurements.

The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons·2026

S-Nitrosylation of glycogen phosphorylase regulates nuclear glycogenolysis and is impaired in metabolic liver disorders.

Science advances·2026

Preimplantation Genetic Testing for FMR1 CGG Repeat Expansions: Clinical and Molecular Aspects in Assisted Reproduction.

JBRA assisted reproduction·2026

Genome sequencing reveals the prevalence of Fabry disease-causing variants in Japan: Evidence from the Tohoku Medical Megabank.

Genetics in medicine open·2026

Chromosome-scale assembly of yeast genomes using enzyme-free, dense optical genome mapping.

Nature communications·2026

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Four examples of the S-s-U-phenotype in an Indian family

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Rh33 in two of three German siblings with D+ C+ c+ E- e+ red cells.

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