DIE ANGEBORENE HYPOTHYREOSE = HYPOTHYROIDIE CONGENITALERABL W.1979; FORTSCHR. D. MED.; DEU; DA. 1979; VOL. 97; NO 6; PP. 225-231; ABS. ENG; BIBL. 20 REF.Article

³H-CYMAROL IN MAN: EXCRETION PATHWAYS AND SERUM PROTEIN BINDING.GUNDERT REMY U; WEBER E; RABL W et al.1978; ARZTL. FORSCH.; DEU; DA. 1978; NO 2; PP. 1174-1176; ABS. GER; BIBL. 7 REF.Article

Kutane LeishmanioseRABL, W; STEYRER, K.Aktuelle Dermatologie. 1991, Vol 17, Num 7, pp 195-198, issn 0340-2541Article

Pulmonary Aspergillus colonization in humans and its impact on management of critically ill patientsLASS-FLÖRL, C; SALZER, G. M; SCHMID, T et al.British journal of haematology. 1999, Vol 104, Num 4, pp 745-747, issn 0007-1048Article

Review of active compression-decompression cardiopulmonary resuscitation (ACD-CPR) : Analysis of iatrogenic complications and their biomechanical explanationRABL, W; BAUBIN, M; HAID, C et al.Forensic science international. 1997, Vol 89, Num 3, pp 175-183, issn 0379-0738Article

Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyKOSUGI, S; VAN DOP, C; GEFFNER, M. E et al.Human molecular genetics (Print). 1995, Vol 4, Num 2, pp 183-188, issn 0964-6906Article

Biomechanical properties of the human tibia : fracture behavior and morphologyRABL, W; HAID, C; KRISMER, M et al.Forensic science international. 1996, Vol 83, Num 1, pp 39-49, issn 0379-0738Article

Embolia Cutis MedicamentosaFÜRNSINN, G; RABL, W; NORDBERG, J et al.Aktuelle Dermatologie. 1990, Vol 16, Num 7, pp 212-213, issn 0340-2541Article

Epidurale Hämatome mit atypischem klinischen Verlauf = Epidural haematomas with atypical clinical manifestationsRABL, W; SIGRIST, T; MARTY, W et al.Der Unfallchirurg. 1993, Vol 96, Num 12, pp 632-635, issn 0177-5537Article

Evaluation of gonadal function in 107 intersex patients by means of serum antimüllerian hormone measurementREY, R. A; BELVILLE, C; BOUVATTIER, C et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 2, pp 627-631, issn 0021-972XArticle

Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancyTHOMAS, P. M; WOHLLK, N; HUANG, E et al.American journal of human genetics. 1996, Vol 59, Num 3, pp 510-518, issn 0002-9297Article

Verlauf, Therapie und Komorbidität bei Hashimoto-Thyreoiditis im Kindesalter = Course, treatment and co-morbidity of hashimoto thyroiditis in 130 children and addolescentsDÖTSCH, J; HAU, M; HEIDEMANN, P et al.Monatsschrift für Kinderheilkunde. 2003, Vol 151, Num 5, pp 528-531, issn 0026-9298, 4 p.Article

Chest injuries after active compression-decompression cardiopulmonary resuscitation (ACD-CPR) in cadaversBAUBIN, M; RABL, W; PFEIFFER, K. P et al.Resuscitation. 1999, Vol 43, Num 1, pp 9-15, issn 0300-9572Article

Delay of Type I diabetes in high risk, first degree relatives by parenteral antigen administration : The Schwabing Insulin Prophylaxis Pilot TrialFÜCHTENBUSCH, M; RABL, W; GRASSL, B et al.Diabetologia (Berlin). 1998, Vol 41, Num 5, pp 536-541, issn 0012-186XArticle

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypodonadismMUSCATELLI, F; STROM, T. M; SCHWARZ, H. P et al.Nature (London). 1994, Vol 372, Num 6507, pp 672-676, issn 0028-0836Article

Diabetes Mellitus in Children and Adolescents with Genetic SyndromesSCHMIDT, F; KAPELLEN, T. M; WIEGAND, S et al.Experimental and clinical endocrinology & diabetes. 2012, Vol 120, Num 10, pp 579-585, issn 0947-7349, 7 p.Article

Chromogranin peptides in amyotrophic lateral sclerosisSCHROTT-FISCHER, A; BITSCHE, M; HUMPEL, C et al.Regulatory peptides. 2009, Vol 152, Num 1-3, pp 13-21, issn 0167-0115, 9 p.Article

Metabolic control as reflectet by HbAlc in children, adolescents and young adults with type-1 diabetes mellitus : combined longitudinal analysis including 27,035 patients from 207 centers in Germany and Austria during the last decadeGERSTL, E.-M; RABL, W; ROSENBAUER, J et al.European journal of pediatrics. 2008, Vol 167, Num 4, pp 447-453, issn 0340-6199, 7 p.Article

Hyperinsulinism in syndromal disordersMEISSNER, T; RABL, W; MOHNIKE, K et al.Acta paediatrica (Oslo). 2001, Vol 90, Num 8, pp 856-859, issn 0803-5253Article

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane proteinSTROM, T. M; HÖRTNAGEL, K; HOFMANN, S et al.Human molecular genetics (Print). 1998, Vol 7, Num 13, pp 2021-2028, issn 0964-6906Article

Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyTHOMAS, P. M; COTE, G. J; WOHLK, N et al.Science (Washington, D.C.). 1995, Vol 268, Num 5209, pp 426-429, issn 0036-8075Article

On the appearance of islet associated autoimmunity in offspring of diabetic mothers : a prospective study from birthZIEGLER, A.-G; HILLEBRAND, B; RABL, W et al.Diabetologia (Berlin). 1993, Vol 36, Num 5, pp 402-408, issn 0012-186XArticle