Literature DB >> 14492555

S-C hemoglobin: a clinical study.

G L RIVER, A B ROBBINS, S O SCHWARTZ.   

Abstract

Keywords:  BLOOD DISEASES; HEMOGLOBIN/abnormalities

Mesh：

Substances：

Year:  1961        PMID： 14492555

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  12 in total

1.  REGULATION OF SPLEEN GROWTH AND SEQUESTERING FUNCTION.

Authors:  H S JACOB; R A MACDONALD; J H JANDL
Journal:  J Clin Invest       Date:  1963-09       Impact factor: 14.808

2.  Hemoglobin sickle cell disease complications: a clinical study of 179 cases.

Authors:  François Lionnet; Nadjib Hammoudi; Katia Stankovic Stojanovic; Virginie Avellino; Gilles Grateau; Robert Girot; Jean-Philippe Haymann
Journal:  Haematologica       Date:  2012-02-07       Impact factor: 9.941

3.  Human bulbar conjunctival hemodynamics in hemoglobin SS and SC disease.

Authors:  Justin Wanek; Bruce Gaynes; Jennifer I Lim; Robert Molokie; Mahnaz Shahidi
Journal:  Am J Hematol       Date:  2013-06-12       Impact factor: 10.047

4.  Acute splenic sequestration crisis in a young woman with homozygous sickle cell anaemia.

Authors:  P S Sarma
Journal:  Postgrad Med J       Date:  1989-02       Impact factor: 2.401

5.  Top-down proteomics and direct surface sampling of neonatal dried blood spots: diagnosis of unknown hemoglobin variants.

Authors:  Rebecca L Edwards; Paul Griffiths; Josephine Bunch; Helen J Cooper
Journal:  J Am Soc Mass Spectrom       Date:  2012-09-20       Impact factor: 3.109

6.  Sickle-cell haemoglobin C disease in London.

Authors:  A J Black; P I Condon; B M Gompels; R L Green; R G Huntsman; G C Jenkins
Journal:  J Clin Pathol       Date:  1972-01       Impact factor: 3.411

7.  Hyposthenuria in sickle cell disease.

Authors:  Y F Francis; H G Worthen
Journal:  J Natl Med Assoc       Date:  1968-07       Impact factor: 1.798

8.  Acute splenic sequestration crisis preceded by hypersplenism in haemoglobin SC disease.

Authors:  J M Topley; D Obeid; J R Mann
Journal:  Br Med J       Date:  1977-03-05

Review 9.  Osteoarticular manifestations in sickle-cell disorders.

Authors:  P Kaklamanis
Journal:  Clin Rheumatol       Date:  1984-12       Impact factor: 2.980

10.  Splenic function in children with hemoglobin SC disease and sickle beta-thalassemia.

Authors:  R H Sills
Journal:  J Natl Med Assoc       Date:  1983-10       Impact factor: 1.798
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