J. Serrat

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

M. Tusié-Luna, P. White, M. New, 1992, The Journal of clinical investigation.

Lipoprotein compositional abnormalities in type I diabetes: effect of improved glycaemic control.

A. de Leiva, D. Mauricio, A. Caixàs, 1997, Diabetes research and clinical practice.

Apolipoprotein C Subtype Distribution in Type 2 Diabetes Mellitus

A. Sorribas, A. Leiva, F. González-Sastre, 1989, Diabetic Medicine.

Plasma Immunoreactive Somatostatin is Elevated in Diabetic Ketoacidosis and Correlates with Plasma Non‐esterified Fatty Acid Concentration

M. Peinado, A. Pérez, A. Leiva, 1987, Diabetic medicine : a journal of the British Diabetic Association.

Apolipoprotein E phenotypes, lipoprotein composition, and xanthelasmas.

F. González-Sastre, J. Serrat, J. A. Gómez, 1988, Archives of dermatology.

Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency.

M. New, P. Speiser, J. Serrat, 1992, The Journal of clinical endocrinology and metabolism.

Evaluation of long-term adherence to oesophagogastroduodenoscopy quality indicators

J. Llach, L. Moreira, G. Fernández-Esparrach, 2020 .

Failure of steroid replacement to consistently normalize pituitary function in congenital adrenal hyperplasia: hormonal and MRI data.

L. Heier, R. Nass, M. New, 1995, Hormone research.