H. Bode

H. Hummler, A. Schulze, A. Flemmer, 2014, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions

F. Bretschneider, H. Lerche, O. Steinlein, 1999, Annals of neurology.

Agranulocytosis associated with lamotrigine

H. Bode, Olaf A Kraus de Camargo, Olaf A Kraus de Camargo, 1999, BMJ.

Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease.

U. Pannicke, K. Schwarz, H. Blom, 2011, American journal of human genetics.

Non‐lethal non‐mosaic male with conradi–hunermann syndrome caused by a novel EBP c.356T>G mutation

H. Hummler, M. Genčík, H. Bode, 2013, American journal of medical genetics. Part A.

Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosum.

Dvir Dahary, P. Nürnberg, T. Hershkovitz, 2013, American journal of human genetics.

Generalized epilepsy with febrile seizures plus

H. Lerche, Y. Weber, A. Ludolph, 2001, Neurology.

Predictive Value of Thompson-Score for Long-Term Neurological and Cognitive Outcome in Term Newborns with Perinatal Asphyxia and Hypoxic-Ischemic Encephalopathy Undergoing Controlled Hypothermia Treatment

H. Hummler, B. Mayer, H. Bode, 2018, Neonatology.

Orofacial Findings in Conjunction with Infantile Cerebral Paralysis in Adults of Two Different Age Groups – a Cross-sectional Study

H. Bode, U. Ehmer, Schirin-Miriam Asdaghi Mamaghani, 2008, Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie.

Intrauterine, Early Neonatal, and Postdischarge Growth and Neurodevelopmental Outcome at 5.4 Years in Extremely Preterm Infants After Intensive Neonatal Nutritional Support

M. Kron, H. Bode, F. Pohlandt, 2009, Pediatrics.

Late onset white matter disease in peroxisome biogenesis disorder

P. Vreken, C. Majoie, P. Barth, 2001, Neurology.

A microdeletion syndrome due to a 3‐Mb deletion on 19q13.2 – Diamond–Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation

H. Cario, E. Kohne, N. Dahl, 1999, Clinical genetics.

CONGENITAL NULL MUTATIONS OF THE FOLR1 GENE: A PROGRESSIVE NEUROLOGIC DISEASE AND ITS TREATMENT

K. Schwarz, H. Cario, K. Debatin, 2009, Neurology.

Dihydrofolate Reductase Deficiency Is Caused by a Homozygous DHFR Mutation and Leads to Congenital Megaloblastic Anemia and Cerebral Folate Deficiency

U. Pannicke, K. Schwarz, H. Blom, 2010 .

Influence of PCO2 Control on Clinical and Neurodevelopmental Outcomes of Extremely Low Birth Weight Infants

J. Dreyhaupt, R. Hentschel, J. Seidenberg, 2018, Neonatology.

Neurodevelopmental outcomes of extremely low birthweight infants randomised to different PCO2 targets: the PHELBI follow-up study

J. Dreyhaupt, R. Hentschel, J. Seidenberg, 2017, Archives of Disease in Childhood: Fetal and Neonatal Edition.

Randomized Trial of Early Versus Late Enteral Iron Supplementation in Infants With a Birth Weight of Less Than 1301 Grams: Neurocognitive Development at 5.3 Years' Corrected Age

M. Kron, H. Bode, F. Pohlandt, 2007, Pediatrics.

Neonatal and neurodevelopmental outcome in infants born before 30 weeks of gestation with absent or reversed end-diastolic flow velocities in the umbilical artery

H. Bode, D. Grab, F. Pohlandt, 2001, European Journal of Pediatrics.

Effect of supplementation with long-chain ω-3 polyunsaturated fatty acids on behavior and cognition in children with attention deficit/hyperactivity disorder (ADHD): a randomized placebo-controlled intervention trial.

H. Bode, Katharina Widenhorn-Müller, Simone Schwanda, 2014, Prostaglandins, leukotrienes, and essential fatty acids.

Type of kindergarten and other potential determinants of overweight in pre-school children

S. Weiland, K. Rapp, H. Bode, 2005, Public Health Nutrition.

Mutations of PTPN23 in developmental and epileptic encephalopathy

F. Alkuraya, S. Arold, H. Thiele, 2017, Human Genetics.

A case of phace syndrome and acquired hypopituitarism?

M. Wabitsch, H. Bode, C. Denzer, 2012, International Journal of Pediatric Endocrinology.

Growth, neurological and cognitive development in infants with a birthweight <501 g at age 5 years

E. Rieger-Fackeldey, H. Bode, A. Schulze, 2010, Acta paediatrica.

Neurodevelopmental follow-up of very preterm infants after proactive treatment at a gestational age of > or = 23 weeks.

M. Kron, H. Bode, F. Pohlandt, 2008, The Journal of pediatrics.

Das therapeutische Repertoir bei Schlafstörungen im Kindesalter: I. Allgemeine Grundsätze und medikamentöse Therapie Therapy of sleep disturbances in childhood and adolescence: I. Principles and pharmacologic therapy

M. Blankenburg, I. Tuxhorn, C. Bönnemann, 2008 .

Generalized epilepsy with febrile seizures plus: Further heterogeneity in a large family

H. Lerche, Y. Weber, A. Ludolph, 2001 .

[Children with learning disabilities and handicaps in inclusive schools or in special schools? The view of parents and professionals].

H. Bode, V. Hirner, 2013, Klinische Pädiatrie.

Entwicklungsneurologische Nachuntersuchung von sehr unreifen Frühgeborenen im Perinatalzentrum Ulm Neurodevelopmental Outcome of Very Low Birth Weight Infants Born at the Perinatal Centre in Ulm, Germany

H. Hummler, H. Bode, S. Sander, 2013 .

H. Bode, Katharina Widenhorn-Müller, Simone Schwanda, 2014, Prostaglandins, leukotrienes, and essential fatty acids.

Complementary/alternative medicine in chronic paediatric diseases--prevalence and parental psychological factors.

H. Bode, M. Storck, O. Müller, 2001, Pediatric rehabilitation.

Entwicklungsneurologische Nachuntersuchung von sehr unreifen Frühgeborenen im Perinatalzentrum Ulm

H. Bode, S. Sander, H. Hummler, 2013, Zeitschrift für Geburtshilfe und Neonatologie.