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Results:
1-17
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Results: 17
BONE-AGE IN 116 UNTREATED PATIENTS WITH TURNERS-SYNDROME RATED BY A COMPUTER-ASSISTED METHOD (CASAS)
Authors:
SCHWARZE CP
ARENS D
HABER HP
WOLLMANN HA
BINDER G
MAYER EIE
RANKE MB
Citation: Cp. Schwarze et al., BONE-AGE IN 116 UNTREATED PATIENTS WITH TURNERS-SYNDROME RATED BY A COMPUTER-ASSISTED METHOD (CASAS), Acta paediatrica, 87(11), 1998, pp. 1146-1150
Authors:
WOLLMANN HA
SCHULTZ U
GRAUER ML
RANKE MB
Citation: Ha. Wollmann et al., REFERENCE VALUES FOR HEIGHT AND WEIGHT IN PRADER-WILLI-SYNDROME BASEDAN 315 PATIENTS, European journal of pediatrics, 157(8), 1998, pp. 634-642
Authors:
WOLLMANN HA
Citation: Ha. Wollmann, INTRAUTERINE GROWTH RESTRICTION - DEFINITION AND ETIOLOGY, Hormone research, 49, 1998, pp. 1-6
Authors:
WOLLMANN HA
Citation: Ha. Wollmann, INTRAUTERINE GROWTH-RETARDATION, Monatsschrift fur Kinderheilkunde, 146(7), 1998, pp. 714-726
Authors:
EGGERMANN T
EGGERMANN K
MERGENTHALER S
KUNER R
KAISER P
RANKE MB
WOLLMANN HA
Citation: T. Eggermann et al., PATERNALLY INHERITED DELETION OF CSH1 IN A PATIENT WITH SILVER-RUSSELL-SYNDROME, Journal of Medical Genetics, 35(9), 1998, pp. 784-786
Authors:
JOEHRER K
GELEY S
STRASSERWOZAK EMC
AZZIZ R
WOLLMANN HA
SCHMITT K
KOFLER R
WHITE PC
Citation: K. Joehrer et al., CYP11B1 MUTATIONS CAUSING NONCLASSIC ADRENAL-HYPERPLASIA DUE TO 11-BETA-HYDROXYLASE DEFICIENCY, Human molecular genetics, 6(11), 1997, pp. 1829-1834
Authors:
EGGERMANN T
WOLLMANN HA
KUNER R
EGGERMANN K
ENDERS H
KAISER P
RANKE MB
Citation: T. Eggermann et al., MOLECULAR STUDIES IN 37 SILVER-RUSSELL-SYNDROME PATIENTS - FREQUENCY AND ETIOLOGY OF UNIPARENTAL DISOMY, Human genetics, 100(3-4), 1997, pp. 415-419
Authors:
HABER HP
WOLLMANN HA
RANKE MB
Citation: Hp. Haber et al., PELVIC ULTRASONOGRAPHY IN SEXUAL PRECOCITY - REPLY, European journal of pediatrics, 156(1), 1997, pp. 79-79
Authors:
EGGERMANN T
WOLLMANN HA
EGGERMANN K
KUNER R
MERGENTHALER S
KAISER P
RANKE MB
Citation: T. Eggermann et al., MOLECULAR STUDIES ON THE ETIOLOGY OF SILVER-RUSSELL-SYNDROME IN 65 PATIENTS, American journal of human genetics, 61(4), 1997, pp. 1796-1796
Authors:
WOLLMANN HA
RANKE MB
Citation: Ha. Wollmann et Mb. Ranke, GH TREATMENT IN NEONATES, Acta paediatrica, 85(4), 1996, pp. 398-400
Authors:
HABER HP
WOLLMANN HA
RANKE MB
Citation: Hp. Haber et al., PELVIC ULTRASONOGRAPHY - EARLY DIFFERENTIATION BETWEEN ISOLATED PREMATURE THELARCHE AND CENTRAL PRECOCIOUS PUBERTY, European journal of pediatrics, 154(3), 1995, pp. 182-186
Authors:
WOLLMANN HA
KIRCHNER T
ENDERS H
PREECE MA
RANKE MB
Citation: Ha. Wollmann et al., GROWTH AND SYMPTOMS IN SILVER-RUSSELL-SYNDROME - REVIEW ON THE BASIS OF 386 PATIENTS, European journal of pediatrics, 154(12), 1995, pp. 958-968
Authors:
RANKE MB
GRAUER ML
KISTNER K
BLUM WF
WOLLMANN HA
Citation: Mb. Ranke et al., SPONTANEOUS ADULT HEIGHT IN IDIOPATHIC SHORT STATURE, Hormone research, 44(4), 1995, pp. 152-157
Authors:
WOLLMANN HA
SCHONAU E
BLUM WF
MEYER F
KRUSE K
RANKE MB
Citation: Ha. Wollmann et al., DOSE-DEPENDENT RESPONSES IN INSULIN-LIKE GROWTH-FACTORS, INSULIN-LIKEGROWTH FACTOR-BINDING PROTEIN-3 AND PARAMETERS OF BONE METABOLISM TO GROWTH-HORMONE THERAPY IN YOUNG-ADULTS WITH GROWTH-HORMONE DEFICIENCY, Hormone research, 43(6), 1995, pp. 249-256
Authors:
WOLLMANN HA
RANKE MB
Citation: Ha. Wollmann et Mb. Ranke, METABOLIC EFFECTS OF GROWTH-HORMONE IN CHILDREN, Metabolism, clinical and experimental, 44(10), 1995, pp. 97-102
Authors:
WOLLMANN HA
RANKE MB
Citation: Ha. Wollmann et Mb. Ranke, BELLS-PALSY AFTER ONSET OF INSULIN-LIKE GROWTH-FACTOR-I THERAPY IN A PATIENT WITH GROWTH-HORMONE RECEPTOR DEFICIENCY, Acta paediatrica, 83, 1994, pp. 148-149
Authors:
WOLLMANN HA
PLEYER U
FRIEDEL S
ZIERHUT M
THIEL HJ
GUPTA D
Citation: Ha. Wollmann et al., NEUROENDOCRINE ALTERATIONS IN UVEITIS PATIENTS, Graefe's archive for clinical and experimental ophthalmology, 232(5), 1994, pp. 297-301
Risultati:
1-17
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