Kleinwuchs

M. Kirchner, V. Hesse:

Beitrag zum Bloom-Syndrom

Humangenetik 15 (1972), 25-32

V. Hesse, M. Kirchner:

Zuordnung von Symptomen zu Syndromen, Symptomatik des Cornelia de Lange-Syndrom

Kinderärztliche Praxis 42 (1974), 263-270

E. Keller, P. Amendt, A. Hempel, V. Hesse, G. K. Hinkel, U. Mix, K. Mohnike, I. Richter, C. Vilser, H. Willgerodt, H. J. Zeisel:

Therapie von Patienten mit hypothalamisch-hypophysärem Minderwuchs mit gentechnisch hergestelltem Wachstumshormon „Saizen“

Zeitschrift für klinische Medizin 45 (1990), 1509-1512

H. Haberland, V. Hesse, R. Schmutzler:

Wachstumsstillstand und Kleinwuchs als erste Zeichen eines Prolaktinoms

Pädiatrische Praxis 54 (1998), 83-88

V. Hesse:

Therapie mit Wachstumshormon: Wirkung und Nebenwirkungen

Kinderärztliche Praxis 72 (2001), 38 – 40

G. Binder, A. Renz, A. Martinez, A. Keselman, V. Hesse, S. W. Riedl, G. Häusler, S. Fricke-Otto, H. Frisch, J. J. Heinrich, M. B. Ranke:

SHOX-Haploinsufficiency and Leri-Weill-Dyschondrosteosis: prevalence and growth failure in relation to mutation, sex and degree of wrist deformity

The Journal of Clinical Endocrinology & Metabolism 89, 2004, 4403-4408

N. T. Hertel, O. Eklof, S. Ivarsson, S. Aronson, O. Westphal, I. Sipila, I. Kaitila, J. Bland, D. Veimo, J. Muller, K. Mohnike, L. Neumeyer, M. Ritzen, L. Hagenas:

Growth hormone treatment in 35 prepubertal children with achondroplasia: a five-year dose-response trial

Acta Paediatrica 94 (10) (2005), 1402-10

Marchini, B. Häcker, T. Marttila, V. Hesse, J. Emons, B. Weiss, M. Karperien, G. Rappold:

BNP is a transcriptional target of the short stature homebox gene SHOX

Human Molecular Genetics 16 (2007), 3081-3087

R. W. Pfaeffle, C. S. Hunter, J. J. Savage, M. Duran-Prado, R. D. Mullen, Z. P. Neeb, U. Eiholzer, V. Hesse, N. G. Haddad, H. M. Stobbe, W. F. Blum, J. F. W. Weigel, S. J. Rhodes:

Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencie

The Journal of Clinical Endocrinology & Metabolism 93 (37, 2008, 1062-1071)

W. F. Blum, D. Cao, V. Hesse, S. Fricke-Otto, J. L. Ross, C. Jones, C. A. Quiglay, G. Binder:

Height gains following GH-treatment to final height are similar in patients with SHOX deficiency and Turner syndrome

Hormone Research in Paediatrics 71 (2009), 167-172

M. Cagnoli, R. Richter, P. Bohm, K. Knye, S. Empting, K. Mohnike:

Spontaneous Growth and Effect of Early Therapy with Calcitriol and Phosphate in X-linked Hypophosphatemic Ricket

Pediatric Endocrinology Reviews 15 (Suppl 1) (2017), 119-122.

E. L. Wakeling, F. Brioude, O. Lokulo-Sodipe, S. M. O’Connell, J. Salem, J. Bliek, A.P. Canton, K. H. Chrzanowska, J. H. Davies, R.P. Dias, B. Dubern, M. Elbracht, E. Giabicani, A. Grimberg, K. Gronskov, A. C. Hokken-Koelega, A.A. Jorge, M. Kagami, A. Linglart, M. Maghnie, K. Mohnike, D. Monk, G. E. Moore, P. G. Murray, T. Ogata, I. O. Petit, S. Russo, E. Said, M. Toumba, Z. Tumer, G. Binder, T. Eggermann, M. D. Harbison, I. K. Temple, D. J. Mackay, I. Netchine:

Diagnosis and management of Silver-Russell syndrome: first international consensus statement

Nature Reviews Endocrinology 13(2) (2017), 105-124.

A. G. Thiele, R. Gausche, C. Lindenberg, C. Beger, M. Arelin, C. Rohde, U. Mutze, J.F. Weigel, K. Mohnike, C. Baerwald, M. Scholz, W. Kiess, R. Pfaffle, S. Beblo:

Growth and Final Height Among Children With Phenylketonuria

Pediatrics 140(5) (2017)

C. Tatsi, A. Gkourogianni, K. Mohnike, D. DeArment, S. Witchel, A. C. Andrade, T. C. Markello, J. Baron, O. Nilsson, Y. H. Jee:

Aggrecan Mutations in Nonfamilial Short Stature and Short Stature Without Accelerated Skeletal Maturation

Journal of the Endocrine Society 1 (8) (2017), 1006-1011.

A. Merker, L. Neumeyer, N. T. Hertel, G. Grigelioniene, K. Mohnike, L. Hagenas:

Development of body proportions in achondroplasia: Sitting height, leg length, arm span, and foot length

American Journal of Medical Genetics Part A 176 (9) (2018), 1819-1829

A. Merker, L. Neumeyer, N.T. Hertel, G. Grigelioniene, O. Makitie, K. Mohnike, L. Hagenas:

Growth in achondroplasia: Development of height, weight, head circumference, and body mass index in a European cohort

American Journal of Medical Genetics Part A 176 (8) (2018), 1723-1734

S. Witt, B. Kolb, J. Bloemeke, K. Mohnike, M. Bullinger, J. Quitmann:

Quality of life of children with achondroplasia and their parents – a German cross-sectional study

Orphanet Journal of Rare Diseases 14 (1) (2019), 194

M. S. Cheung, I. Alves, L. Hagenas, K. Mohnike:

Meeting report from the achondroplasia foramen magnum workshop

Salzburg, Austria 22nd June 2019, Bone 127 (2019), 499-502
DOI 10.1016/j.bone.2019.07.020

J. Quitmann, J. Bloemeke, N. Silva, M. Bullinger, S. Witt, I. Akkurt, D. Dunstheimer, C. Vogel, V. Bottcher, U. Kuhnle Krahl, M. Bettendorf, E. Schonau, S. Fricke-Otto, A. Keller, K. Mohnike, H. G. Dorr:

Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment

Frontiers in Pediatrics 7 (2019), 164

J. Bloemeke, R. Sommer, S. Witt, M. Bullinger, C. Nordon, F. J. Badia, F. L. Gonzalez, A. Leiva-Gea, F. B. Delgado Rufino, F. Mayoral-Cleries, P. Romero-Sanchiz, V. Clamagirand Saiz, R. Nogueira-Arjona, K. Mohnike, J. Quitmann:

Cross-cultural selection and validation of instruments to assess patient-reported outcomes in children and adolescents with achondroplasia

Quality of Life Research28 (9) (2019), 2553-2563.

Hochwuchs

W. Hoepffner, G. Göretzlehner, V. Hesse, E. Keller, K. Mohnike, H. Willgerodt:

Standpunkt zur Hochwuchsbehandlung 1989

Pädiatrie und Grenzgebiete 29 (1990), 193-196

J. Donczik, U. Pankow, V. Hesse:

Einschätzung der psychischen Situation Hochwüchsiger im Erwachsenenalter, Kontrolluntersuchungen ehemals hochwüchsiger Kinder

Pädiatrie und Grenzgebiete 29 (1990), 149-152

H. Vogel, C. Vilser, V. Hesse:

Paraklinische Kontrolluntersuchungen während der Hochwuchstherapie

Pädiatrie und Grenzgebiete 29 (1990), 175-178

E. Kauf, V. Hesse, H. Vogel, C. Vilser:

Mineralstoffwechsel unter Hochwuchstherapie

Pädiatrie und Grenzgebiete 29 (1990), 179-183

S. Turkmen, G. Gillessen-Kaesbach, P. Meinecke, B. Albrecht, L. M. Neumann, V. Hesse, S. Palanduz, S. Balg, F. Majewski, S. Fuds, P. Zschieschang, M. Greiwe, Mennicke, U. A. Mau, H. J. Dehmel, J. Kunze, S. Tinschert, S. Mundlos, D. Horn:

NSD1 mutations are responsible for Sotos syndrome, but not present in Warver syndrome or other overgrowth phenotypes

European Journal of Human Genetics (2003), 858-865