SEVERE PURPURA FULMINANS DUE TO COEXISTENCE OF HOMOZYGOUS PROTEIN C DEFICIENCY AND HOMOZYGOUS METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION

By Demirel Nihal   Bas Ahmet Yagmur   Okumus Nurullah   Zenciroglu Ayşegul   Yarali Nese  

Pediatric Hematology and Oncology, Vol. 26, Iss. 8, 2009-11 ,pp. : 597-600

Informa Healthcare

Access to resources Recommend Favorite

Severe Protein S Deficiency Associated with Heterozygous Factor V Leiden Mutation in a Child with Purpura Fulminans

By Dogan Yasar   Aygun Denizmen   Yılmaz Yelda   Kanra Guler   Secmeer Gulten   Besbas Nesrin   Gurgey Aytemiz  

Pediatric Hematology and Oncology, Vol. 20, Iss. 1, 2003-01 ,pp. : 1-5

Informa Healthcare

Access to resources Recommend Favorite

NEONATAL PURPURA FULMINANS SECONDARY TO GROUP B STREPTOCOCCAL INFECTION

By Zenciroglu Aysegul   Karagol Belma Saygili   Ipek Mehmet Sah   Okumus Nurullah   Yarali Nese   Aydin Mustafa  

Pediatric Hematology and Oncology, Vol. 27, Iss. 8, 2010-10 ,pp. : 620-625

Informa Healthcare

Access to resources Recommend Favorite

Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation

By Spiegel R.   Shaag A.   Gutman A.   Korman S.   Saada A.   Elpeleg O.   Shalev S.  

Journal of Inherited Metabolic Disease, Vol. 30, Iss. 2, 2007-04 ,pp. : 266-266

Springer Publishing Company

Access to resources Recommend Favorite

Neonatal Hypercalcemia due to a Homozygous Mutation in the Calcium-Sensing Receptor: Failure of Cinacalcet

By  

Neonatology, Vol. 104, Iss. 2, 2013-06 ,pp. : 104-108

Karger

Access to resources Recommend Favorite