Ahti Lammi - Concepedia

Author

Ahti Lammi

Children's Hospital at Westmead

Also Known As

A Lammi, AHTI T. LAMMI, Ahti Lammi, Ahti T Lammi, Ahti T. Lammi

Publications

937

Citations

H-Index

Concepts

All Affiliations

Children's Hospital at Westmead The University of Sydney Sydney South West Area Health Service

About

Ahti Lammi is an author at Children's Hospital at Westmead specializing in medicine, hematology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	837
2	Immunology	2	2	177
3	Public Health	1	1	63
4	Child Development	1	1	63
5	Hepatology	1	1	158

Ahti Lammi

Publications

915

Citations

H-Index

Page 1

	Year	Citations
A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction Howard A. Pearson, Jeffrey S. Lobel, Samuel A. Kocoshis, The Journal of Pediatrics AnemiaBone Marrow FailureHematologyBlood CellPathology	1979	440
Chimerism and Tolerance in a Recipient of a Deceased-Donor Liver Transplant Stephen I. Alexander, Neil Smith, Min Hu, New England Journal of Medicine Transplant RejectionOrgan DonationTransplantationHepatologyAutoimmune Disease	2008	158
Idiopathic thrombocytopenic purpura: An epidemiologic study Ahti Lammi, Vladimira Lovrić The Journal of Pediatrics ThrombopoiesisThrombosisVenous ThrombosisAutoimmune DiseaseBlood Platelet	1973	72
Recombinant activated factor VII in paediatric cardiac surgery Jonathan R. Egan, Ahti Lammi, David Schell, Intensive Care Medicine Heart FailureCardiovascular DiseaseFactor ViiPediatric Cardiac SurgeryCongenital Heart Defect	2004	67
Iron status and anaemia in preschool children in Sydney Margaret Karr, Garth Alperstein, Jane Causer, Australian and New Zealand Journal of Public Health AnemiaNutritionPediatric HematologyMedicinePediatrics	1996	63
Human triosephosphate isomerase deficiency resulting from mutation of Phe-240. Min Ling Chang, Peter J. Artymiuk, Xiaoyun Wu, PubMed	1993	51
Iron deficiency in Australian‐born children of Arabic background in central Sydney Margaret Karr, Michael Mira, Garth Alperstein, The Medical Journal of Australia	2001	27
INTERMITTENT 20q- AND CONSISTENT i(7q) IN A PATIENT WITH SHWACHMAN-DIAMOND SYNDROME Arabella Smith, Peter J. Shaw, Boyd Webster, Pediatric Hematology and Oncology Hematological MalignancyChromatinMixed-phenotype Acute LeukemiaGeneticsIntermittent 20Q-	2002	19
The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families Arthur S. Schneider, Beryl Westwood, Catherine Yim, Blood Cells Molecules and Diseases Common HaplotypeAllelic VariantGenetic DisorderGeneticsTriosephosphate Isomerase	1996	18

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