Association of HLA alleles and haplotypes with CYP21A2 gene p. V282L mutation in the Croatian population von Grubic, Z., Maskalan, M., Stingl Jankovic, K., Zvecic, S., Dumic Kubat, K., Krnic, N., Zunec, R., Ille, J., Kusec, V., Dumic, M.

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Low bone mineral density for age/osteoporosis in triple A syndrome—an overlooked symptom of unexplained etiology von Dumic, M., Putarek, N. R., Kusec, V., Barisic, N., Koehler, K., Huebner, A.

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Characteristics of the craniofacial complex in Turner syndrome von Dumancic, J, Kaic, Z, Varga, M. Lapter, Lauc, T, Dumic, M, Milosevic, S. Anic, Brkic, H

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Alicyclic beta-amino acids in Medicinal Chemistry von Kuhl, A, Hahn, M G, Dumić, M, Mittendorf, J

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Bone mineral density in children and young adults with Type 1 diabetes mellitus von Kusec, V, Rojnic-Putarek, N, Ille, J, Radica, A, Jurasinovic, Z, Dumic, M

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4″- O-(ω-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens von Fajdetić, A., Čipčić Paljetak, H., Lazarevski, G., Hutinec, A., Alihodžić, S., Đerek, M., Štimac, V., Andreotti, D., Šunjić, V., Berge, J.M., Mutak, S., Dumić, M., Lociuro, S., Holmes, D.J., Maršić, N., Eraković Haber, V., Spaventi, R.

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Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome) von Zenker, Martin, Mayerle, Julia, Lerch, Markus M, Tagariello, Andreas, Zerres, Klaus, Durie, Peter R, Beier, Matthias, Hülskamp, Georg, Guzman, Celina, Rehder, Helga, Beemer, Frits A, Hamel, Ben, Vanlieferinghen, Philippe, Gershoni-Baruch, Ruth, Vieira, Marta W, Dumic, Miroslav, Auslender, Ron, Gil-da-Silva-Lopes, Vera L, Steinlicht, Simone, Rauh, Manfred, Shalev, Stavit A, Thiel, Christian, Winterpacht, Andreas, Kwon, Yong Tae, Varshavsky, Alexander, Reis, André

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Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Without Demonstrable Genetic Mutations von Nimkarn, S., Cerame, B. I., Wei, J.-Q., Dumic, M., Z̈unec, R., Brkljacic, L., S̆krabic, V., New, M. I., Wilson, R. C.

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Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome von Grant, D B, Barnes, N D, Dumic, M, Ginalska-Malinowska, M, Milla, P J, von Petrykowski, W, Rowlatt, R J, Steendijk, R, Wales, J H, Werder, E

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Long Term Follow-Up of Clinical and Electromyoneurographical Abnormalities in Eight Croatian Patients with Triple A Syndrome (P01.126) von Barisic, N., Dumic, M., Kusec, V., Stingl, K., Lehman, I., Bunoza, B., Grdan, P., Koehler, K., Heubner, A.

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Thyroid diseases in a school population with thyromegaly von Jaksić, J, Dumić, M, Filipović, B, Ille, J, Cvijetić, M, Gjurić, G

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O46 – 1548 Long term follow-up of clinical and neurographical abnormalities in eight Croatian patients with triple A syndrome von Barisic, N, Dumic, M, Kusec, V, Lehman, I, Bunoza, B, Grdjan, P, Ivanja, V

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Xerostomia in patients with triple A syndrome : a newly recognised finding von DUMIC, Miroslav, MRAVAK-STIPETIC, Marinka, KAIC, Zvonimir, ILLE, Jasenka, PLAVSIC, Vesna, BATINICA, Stipe, CVITANOVIC, Marijana

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Eur J Pediatr.: Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy von Kusec, V, Stanimirovic, A, Barisic, N, Dumic, M, Huebner, A, Koehler, K, Rojnic-Putarek, N

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Alicyclic [beta]-amino acids in Medicinal Chemistry von Kuhl, A, Hahn, M G, Dumic, M, Mittendorf, J

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Apolipoprotein E phenotypes and genotypes as determined by polymerase chain reaction using allele-specific oligonucleotide probes and the amplification refractory mutation system i... von Stavljenic-Rukavina, A., Sertic, J., Salzer, B., Dumic, M., Radica, A., Fumic, K., Krajina, A.

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Antihyperglycemic N-sulfonyl-1a,2,6,6a-tetrahydro-1H,4H- [1,3]dioxepino[5,6-b]azirines: synthesis, X-ray structure analysis, conformational behavior, quantitative structure-propert... von Dumić, M, Vinković, M, Filić, D, Jamnicky, B, Eskinja, M, Kamenar, B

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Synthesis, Characterization and In Vitro Antimicrobial Activity of Novel Sulfonylureas of 15-Membered Azalides von Krajačić, Mirjana Bukvić, Kujundžić, Nedjeljko, Dumić, Miljenko, Cindrić, Mario, Brajša, Karmen, Metelko, Biserka, Novak, Predrag

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Bilateral gonadoblastoma in a 9-month-old infant with 46,XY gonadal dysgenesis von Dumić, M, Jukić, S, Batinica, S, Ille, J, Filipović-Grcić, B

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Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders von DUMIC, M, RADICA, A, SABOL, Z, PLAVSIC, V, BRKLJACIC, L, SARNAVKA, V, VUKOVIC, J

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