C. Knopf

发表

SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4.

H. Mandel, M. Indelman, E. Sprecher, 2008, American journal of human genetics.

RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome.

O. Sarig, A. Ishida-Yamamoto, H. Hennies, 2009, American journal of human genetics.

11β–Hydroxysteroid Dehydrogenase Type 1 Activity in Short Small-For-GA Children and in Response to GH Therapy

Z. Hochberg, N. Zuckerman-Levin, Z. Shen-Orr, 2011, Pediatric Research.

A steroid metabolomic approach to 17α-hydroxylase/17,20 lyase deficiency

Z. Yakhini, Z. Hochberg, R. Navon, 2010, Metabolomics.

Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicism

H. Mandel, M. Berant, R. Gershoni-baruch, 2000, Journal of Inherited Metabolic Disease.

The influence of pentoxyfylline [1-(5-oxohexyl-) 3,7-dimethylxanthine] (BL 191) on the insulin secretion induced by glibenclamide and by arginine/glucose in the perfused pancreas

D. Udrisar, C. Knopf, N. Aparicio, 1977, Acta diabetologia latina.

Angiotensin II reduces macrophage cholesterol efflux: a role for the AT-1 receptor but not for the ABC1 transporter.

M. Aviram, C. Knopf, S. Keidar, 2002, Biochemical and biophysical research communications.

Influence of co-administration of oral insulin and docosahexaenoic acid in mice.

H. Mandel, R. Shamir, N. Shehadeh, 2004, The Journal of nutritional biochemistry.

Metabolic evidence for impaired 17alpha-hydroxylase activity in a kindred bearing the E305G mutation for isolate 17,20-lyase activity.

Z. Hochberg, D. Tiosano, M. Hartmann, 2008, European journal of endocrinology.

Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation

J. Schuurs-Hoeijmakers, H. Mandel, J. van Reeuwijk, 2011, PLoS genetics.

The Liver in Congenital Disorders of Glycosylation: Ultrastructural Features

H. Mandel, M. Mahajnah, Irena Manov, 2007, Ultrastructural pathology.

Oral glucose tolerance test in 100 normal children

J. Cresto, C. Knopf, I. Dujovne, 1977, Acta diabetologia latina.

Cortisol-Metabolizing Enzymes in Polycystic Ovary Syndrome

Z. Hochberg, Z. Blumenfeld, C. Knopf, 2016, Clinical medicine insights. Reproductive health.