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Giant Platelet Count (procedure)
Known as:
Giant Platelet Count
, Giant Platelets
, PLATGNT
The determination of the number of giant platelets present in a sample.
National Institutes of Health
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Related topics
Related topics
3 relations
CDISC SDTM Laboratory Test Terminology by Code
CDISC SDTM Laboratory Test Terminology by Name
Clinical Data Interchange Standards Consortium Terminology
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Immune Thrombocytopenia Induced by Nivolumab in a Metastatic Non-Small Cell Lung Cancer Patient
Y. Karakaş
,
D. Yuce
,
S. Kılıçkap
Oncology Research and Treatment
2017
Corpus ID: 207653255
phy and cranial magnetic resonance imaging were performed for staging. The tumor was shown to have invaded the third rib, the…
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2009
2009
A large Swiss family with Bernard-Soulier syndrome
B. Zieger
,
A. Jenny
,
+6 authors
W. Wuillemin
Hämostaseologie
2009
Corpus ID: 24435984
Summary Bernard-Soulier syndrome (BSS) is a rare, autosomal recessive inherited bleeding disorder associated with…
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Highly Cited
2008
Highly Cited
2008
Reticulocyte count using thiazole orange. A flow cytometry method.
L. V. D. hove
,
Willy Goossens
,
Van Duppen
,
R. Verwilghen
Clinical and Laboratory Haematology
2008
Corpus ID: 22035669
Recently flow cytometry techniques have been developed to replace the microscope reticulocyte count. We used thiazole orange, a…
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Highly Cited
2003
Highly Cited
2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.
S. Deutsch
,
A. Rideau
,
+7 authors
P. Beris
Blood
2003
Corpus ID: 14983469
May-Hegglin anomaly (MHA), Fechtner syndrome (FTNS), Sebastian syndrome (SBS), and Epstein syndrome (EPS) are a group of rare…
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2000
2000
Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13.
A. Toren
,
G. Rozenfeld-Granot
,
+8 authors
A. Greinacher
Blood
2000
Corpus ID: 7930749
Families with 3 different syndromes characterized by autosomal dominant inheritance of low platelet count and giant platelets…
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1999
1999
Compound Heterozygosity (554-589 del, C515-T Transition) in the Platelet Glycoprotein Ibα Gene in a Patient with a Severe Bleeding Tendency
M. Margaglione
,
G. D’Andrea
,
E. Grandone
,
V. Brancaccio
,
A. Amoriello
,
G. Di Minno
Thrombosis and Haemostasis
1999
Corpus ID: 37273969
Summary Giant platelets in the blood smear, absent in vitro platelet agglutination in response to ristocetin, and normal…
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1998
1998
Giant platelet disorder in a patient with type 2B von Willebrand's disease
S. Moll
,
Alicia Rico Lazarowski
,
G. White
American journal of hematology/oncology
1998
Corpus ID: 8898350
While patients with type 2B von Willebrand's disease often exhibit thrombocytopenia, platelet morphology is typically normal. We…
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1996
1996
Physician Education: Myelodysplastic Syndrome.
Y. Yoshida
The Oncologist
1996
Corpus ID: 39998059
CHARACTERISTICS AND PATHOLOGY OF MYELODYSPLASTIC SYNROME: Myelodysplastic syndrome (MDS) is a disease of the blood whose etiology…
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Highly Cited
1994
Highly Cited
1994
Cys209 Ser mutation in the platelet membrane glycoprotein ibα gene is associated with Bernard‐Soulier syndrome
S. Simsek
,
P. Noris
,
+4 authors
D. Gallardo
British Journal of Haematology
1994
Corpus ID: 25763861
Summary Molecular genetic analysis has been performed on a patient with Bernard‐Soulier syndrome (BSS). The patient had…
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1991
1991
Coronary thrombosis in a patient with May-Hegglin anomaly.
S. Mcdunn
,
W. Hartz
,
C. Ts'ao
,
D. Green
American Journal of Clinical Pathology
1991
Corpus ID: 8210005
May-Hegglin anomaly (MHA) is a rare hereditary condition that is characterized by cytoplasmic inclusions in leukocytes and giant…
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