J. Pohlenz

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Cryptosporidiosis as a probable factor in neonatal diarrhea of calves.

N. Cheville, H. Moon, W. J. Bemrick, 1978, Journal of the American Veterinary Medical Association.

Bovine Cryptosporidiosis: A Transmission and Scanning Electron Microscopic Study of Some Stages in the Life Cycle and of the Host-Parasite Relationship

N. Cheville, H. Moon, W. J. Bemrick, 1978, Veterinary pathology.

Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes.

A. Turk, P. Kopp, G. Borck, 2006, The Journal of clinical endocrinology and metabolism.

Intrafamilial variability of the deafness and goiter phenotype in Pendred syndrome caused by a T416P mutation in the SLC26A4 gene.

G. Borck, A. Keilmann, N. Pfarr, 2004, The Journal of clinical endocrinology and metabolism.

Pathogenic relationships of rotavirus, Escherichia coli, and other agents in mixed infections in calves.

R. Isaacson, H. Moon, J. Pohlenz, 1978, Journal of the American Veterinary Medical Association.

Determination of thyroid volume in infants with suspected congenital hypothyroidism—the limitations of both subjective and objective evaluation

M. Donaldson, G. Irwin, J. Jones, 2020, BJR open.

Staining of Cryptosporidia by a Modified Ziehl-Neelsen Technique

J. Pohlenz, S. Henriksen, 1981, Acta Veterinaria Scandinavica.

Impaired iloprost-induced platelet inhibition and phosphoproteome changes in patients with confirmed pseudohypoparathyroidism type Ia, linked to genetic mutations in GNAS

R. Zahedi, A. Sickmann, C. Stumpel, 2020, Scientific Reports.

Comparative Pathogenicity of Escherichia coli O157 and Intimin-Negative Non-O157 Shiga Toxin-Producing E. coli Strains in Neonatal Pigs

H. Moon, A. O’Brien, A. Melton-Celsa, 2003, Infection and Immunity.

Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studies.

J. Parma, G. Vassart, S. Biesterfeld, 2008, The Journal of clinical endocrinology and metabolism.

Congenital Deafness and Goiter: Pendred Syndrome

G. Borck, A. Keilmann, W. Müller-Forell, 2006 .

Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10‐bp deletion in the thyroid peroxidase (TPO) gene

T. Musholt, R. Brzezińska, N. Pfarr, 2006, Clinical endocrinology.

Thyroid surgery in children and young adults: potential overtreatment and complications

T. Musholt, H. Lang, J. Bode, 2020, Langenbeck's Archives of Surgery.

Intrathyroidal thymic tissue surrounding an intrathyroidal parathyroid gland, the cause of a solitary thyroid nodule in a 6-year-old boy.

T. Musholt, R. Brzezińska, A. Kreft, 2008, Thyroid : official journal of the American Thyroid Association.

Missense mutations of dual oxidase 2 (DUOX2) implicated in congenital hypothyroidism have impaired trafficking in cells reconstituted with DUOX2 maturation factor.

F. Miot, S. Refetoff, X. de Deken, 2007, Molecular endocrinology.

Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation

O. Fuchs, H. Schmidt, N. Pfarr, 2009, Developmental medicine and child neurology.

Early Epithelial Invasion by Salmonella enterica Serovar Typhimurium DT104 in the Swine Ileum

D. Meyerholz, M. Ackermann, S. Carlson, 2002, Veterinary pathology.

A new PAX8 mutation causing congenital hypothyroidism in three generations of a family is associated with abnormalities in the urogenital tract.

R. Cabral, L. Mota-Vieira, H. Bikker, 2013, Thyroid : official journal of the American Thyroid Association.

A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studies

S. Refetoff, Chutintorn Sriphrapradang, A. Slyper, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

Minimally invasive follicular thyroid carcinoma developed in dyshormonogenetic multinodular goiter due to thyroid peroxidase gene mutation.

Y. Tenenbaum‐Rakover, A. Ishay, J. Pohlenz, 2012, Thyroid : official journal of the American Thyroid Association.

Thyroid Peroxidase Gene Mutations Causing Congenital Hypothyroidism in Three Turkish Families

B. Yuksel, M. Ozbek, N. Onenli-Mungan, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children

H. Dörr, D. Prawitt, N. Pfarr, 2009, Acta paediatrica.

Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis

J. Sack, C. Ris-Stalpers, S. Refetoff, 2007, Clinical endocrinology.

Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene

A. Herbst, S. Kaspers, N. Pfarr, 2006, Clinical endocrinology.

Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters.

S. Costagliola, G. Vassart, R. Weiss, 2000, The Journal of clinical endocrinology and metabolism.

Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site.

C. Burant, S. Jhiang, R. Weiss, 1998, The Journal of clinical investigation.

Improved radioimmunoassay for measurement of mouse thyrotropin in serum: strain differences in thyrotropin concentration and thyrotroph sensitivity to thyroid hormone.

R. Weiss, S. Refetoff, J. van Sande, 1999, Thyroid : official journal of the American Thyroid Association.

A novel point mutation in cluster 3 of the thyroid hormone receptor beta gene (P247L) causing mild resistance to thyroid hormone.

R. Weiss, S. Refetoff, P. Sadow, 1999, Thyroid : official journal of the American Thyroid Association.

A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones

O. Hiort, J. Winter, J. Pohlenz, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

with Cryptosporidium Species

J. Heine, H. Moon, J. Pohlenz, 1984 .

Enteric Lesions and Diarrhea in Gnotobiotic Calves Monoinfected with Cryptosporidium Species

J. Heine, H. Moon, J. Pohlenz, 1984, The Journal of infectious diseases.

Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene.

P. Macchia, R. Weiss, S. Refetoff, 1999, The Journal of clinical endocrinology and metabolism.

Long-Term Carbimazole Treatment of Neonatal Nonautoimmune Hyperthyroidism due to a New Activating TSH Receptor Gene Mutation (Ala428Val)

H. Koch, J. Pohlenz, Kirsten Börgel, 2005, Hormone Research in Paediatrics.

Saccharomyces boulardii and bacillus cereus var. Toyoi influence the morphology and the mucins of the intestine of pigs.

G. Breves, E. Liebler-Tenorio, M. Enss, 2002, Zeitschrift fur Gastroenterologie.

Immunohistochemical demonstration of African horse sickness viral antigen in tissues of experimentally infected equines.

P. Wohlsein, J. Salt, C. Hamblin, 1998, Archives of virology. Supplementum.

Distribution of cytopathogenic and noncytopathogenic bovine virus diarrhea virus in tissues from a calf with experimentally induced mucosal disease using antigenic and genetic markers.

V. Moennig, B. Liess, I. Greiser-Wilke, 1993, Archives of virology. Supplementum.

Influence of breed-related factors on the course of classical swine fever virus infection

V. Moennig, K. Depner, B. Liess, 1997, Veterinary Record.

[Spongiform encephalopathy in a red-necked ostrich (Struthio camelus)].

D. Brunckhorst, J. Pohlenz, H. Schoon, 1991, Tierarztliche Praxis.

Immunohistochemical Demonstration of African Horse Sickness Viral Antigen in Formalin-fixed Equine Tissues

P. Wohlsein, J. Salt, C. Hamblin, 1997, Veterinary pathology.

Uptake of Ferritin by Follicle-associated Epithelium in the Colon of Calves

J. Pohlenz, M. Paar, E. Liebler, 1992, Veterinary pathology.

An improved DNA test for bovine leucocyte adhesion deficiency.

B. Harlizius, D. Simon, J. Pohlenz, 1996, Research in veterinary science.

Escherichia coli O157:H7 Causes More-Severe Systemic Disease in Suckling Piglets than in Colostrum-Deprived Neonatal Piglets

H. Moon, A. O’Brien, J. Pohlenz, 2000, Infection and Immunity.

Early Attachment Sites for Shiga-Toxigenic Escherichia coli O157:H7 in Experimentally Inoculated Weaned Calves

B. Bosworth, H. Moon, W. Stoffregen, 2008, Applied and Environmental Microbiology.

Shiga-Toxigenic Escherichia coli-Inoculated Neonatal Piglets Develop Kidney Lesions That Are Comparable to Those in Humans with Hemolytic-Uremic Syndrome

J. Pohlenz, E. Dean-Nystrom, K. Winter, 2005, Infection and Immunity.

Escherichia coli O157:H7 in the Gallbladders of Experimentally Infected Calves

W. Stoffregen, J. Pohlenz, E. Dean-Nystrom, 2004, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

Bacterial Colonization and Morphology of the Intestine in Porcine Escherichia Coli Enterotoxemia (Edema Disease)

J. Pohlenz, H. Bertschinger, 1983, Veterinary pathology.

Enhancer Mutation Linking C5 Deficiency to an Exonic Splicing

W. Fairbrother, M. Kirschfink, F. Zepp, 2005 .

This information is current as Enhancer Mutation Linking C 5 Deficiency to an Exonic Splicing

C. Burge, W. Fairbrother, D. Prawitt, 2005 .

A Novel Deletion in the Thyrotropin Beta-Subunit Gene Identified by Array Comparative Genomic Hybridization Analysis Causes Central Congenital Hypothyroidism in a Boy Originating from Turkey

N. Leonard, R. Couch, Cherise M. Klotz, 2014, Hormone Research in Paediatrics.

Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.

G. Borck, A. Topaloğlu, B. Yuksel, 2004, The Journal of clinical endocrinology and metabolism.

Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritance.

R. Pfäffle, W. Andler, J. Pohlenz, 1998, The Journal of clinical endocrinology and metabolism.

A De Novo Mutation in an Already Mutant Nucleotide of the Thyroid Hormone Receptor β Gene Perpetuates Resistance to Thyroid Hormone

A. Verloes, R. Weiss, S. Refetoff, 2005 .

Changes in distribution and numbers of CD4+ and CD8+ T-lymphocytes in lymphoid tissues and intestinal mucosa in the early phase of experimentally induced early onset mucosal disease in cattle.

E. Liebler-Tenorio, B. Grummer, J. Pohlenz, 2002, Journal of veterinary medicine. B, Infectious diseases and veterinary public health.

Experimental mucosal disease in cattle: changes in the number of lymphocytes and plasma cells in the mucosa of the small and large intestine.

J. Pohlenz, E. Liebler, C. Küsters, 1996, Veterinary immunology and immunopathology.

Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' disease.

S. Costagliola, G. Vassart, S. Refetoff, 2000, The Journal of clinical investigation.

Subclinical cryptosporidiosis of turkeys in Iowa.

H. Moon, J. Pohlenz, D. Woodmansee, 1988, The Journal of parasitology.

Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R)

V. Hesse, N. Pfarr, J. Pohlenz, 2006, Acta paediatrica.

Detection of Papillary Thyroid Carcinoma by Analysis of BRAF and RET/PTC1 Mutations in Fine-needle Aspiration Biopsies of Thyroid Nodules

Matthias M. Weber, T. Musholt, A. Schad, 2010, World Journal of Surgery.

Morphologic lesions in type 2 BVDV infections experimentally induced by strain BVDV2-1373 recovered from a field case.

J. Ridpath, S. Bolin, J. Pohlenz, 2000, Veterinary microbiology.

A new mutation in the promoter region of the PAX8 gene causes true congenital hypothyroidism with thyroid hypoplasia in a girl with Down's syndrome.

J. Schulga, M. Donaldson, J. Pohlenz, 2014, Thyroid : official journal of the American Thyroid Association.

Mechanisms of association of enteropathogenic Escherichia coli with intestinal epithelium.

R. Isaacson, H. Moon, J. Pohlenz, 1979, The American journal of clinical nutrition.

Morphological and immunohistochemical characterization of spontaneous mammary tumours in European hedgehogs (Erinaceus europaeus).

P. Wohlsein, M. Fehr, J. Pohlenz, 2007, Journal of comparative pathology.

Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis.

S. Refetoff, H. Grasberger, J. Pohlenz, 2011, The Journal of clinical endocrinology and metabolism.

Chapter 8 – Developmental Abnormalities of the Thyroid

J. Deladoëy, G. Vliet, J. Pohlenz, 2016 .

Developmental Abnormalities of the Thyroid

G. Vliet, J. Pohlenz, 2010 .

Pathomorphological and immunohistological findings in cattle experimentally infected with rinderpest virus isolates of different pathogenicity.

P. Wohlsein, H. Wamwayi, T. Barrett, 1995, Veterinary microbiology.

Congenital Central Hypothyroidism due to a Homozygous Mutation in the TSHβ Subunit Gene

M. Schmidts, S. Grünert, K. Schwab, 2011, Case reports in pediatrics.

Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene.

D. Prawitt, S. Refetoff, A. Dumitrescu, 2002, The Journal of clinical endocrinology and metabolism.

A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa

F. Asmus, T. Gasser, A. Zimprich, 2005, Neurology.

Diagnostic and predictive value of ultrasound and isotope thyroid scanning, alone and in combination, in infants referred with thyroid-stimulating hormone elevation on newborn screening.

M. Donaldson, A. Lucas-Herald, J. Jones, 2014, The Journal of pediatrics.

[On the effect of mebendazole on metacestodes of Mesocestoides corti and Echinococcus multilocularis (author's transl)].

J. Eckert, J. Pohlenz, 1976, Tropenmedizin und Parasitologie.

Vitamin D intoxication in Airedale puppies fed with milk replacer.

J. Kamphues, J. Pohlenz, W. Wirth, 1990 .

Idiopathic systemic granulomatous disease with encephalitis in a horse.

J. Pohlenz, M. Peters, G. Graf, 2003, Journal of veterinary medicine. A, Physiology, pathology, clinical medicine.

Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria.

B. Brenig, J. Pohlenz, A. Seubert, 2005, Animal genetics.

[Measurement of glomerular filtration rate (GFR) after administration of iodine contrast medium with the Renalyzer PRX90 in healthy cats and cats with kidney diseases].

I. Nolte, P. Wohlsein, A. Meyer-Lindenberg, 1998, Berliner und Munchener tierarztliche Wochenschrift.

[Experimental infestation of cattle with ectoparasites and their effect on leather quality].

A. von Rotz, M. Suter, J. Pohlenz, 1983, Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B.

Spontaneous Plasma Cell Myeloma in a Ferret (Mustela putorius furo)

R. Myers, J. Pohlenz, S. Methiyapun, 1985, Veterinary pathology.

Intestinal lesions in experimental phocine distemper: light microscopy, immunohistochemistry and electron microscopy.

P. Wohlsein, J. Pohlenz, G. Pohlmeyer, 1993, Journal of comparative pathology.

Comparative investigation of tissue alterations and distribution of BVD-viral antigen in cattle with early onset versus late onset mucosal disease.

B. Loehr, E. Liebler-Tenorio, I. Greiser-Wilke, 2000, Veterinary microbiology.

Experimental tracheal and conjunctival infections with Cryptosporidium sp. in pigs.

J. Heine, H. Moon, J. Pohlenz, 1984, Veterinary parasitology.

Isolation of mycoplasmas from diseased seals

B. Liess, J. Pohlenz, K. Friedhoff, 1989, Veterinary Record.

Astrovirus and Breda virus infections of dome cell epithelium of bovine ileum

J. Pohlenz, G. Woode, J. Fagerland, 1984, Journal of clinical microbiology.

Experimental mucosal disease in cattle: changes of lymphocyte subpopulations in Peyer's patches and in lymphoid nodules of large intestine.

J. Pohlenz, E. Liebler, C. Küsters, 1995, Veterinary immunology and immunopathology.

Organ and tissue distribution of the antigen of thecytopathogenic bovine virus diarrhea virus in theearly and advanced phase of experimentalmucosal disease

E. Liebler-Tenorio, I. Greiser-Wilke, J. Pohlenz, 1997, Archives of Virology.

Distribution of antigen of noncytopathogenic and cytopathogenic bovine virus diarrhea virus biotypes in the intestinal tract of calves following experimental production of mucosal disease.

V. Moennig, B. Liess, J. Pohlenz, 1991, Archives of virology. Supplementum.

Incidence of BVDV1 and BVDV2 infections in cattle submitted for necropsy in Northern Germany.

E. Liebler-Tenorio, B. Makoschey, I. Greiser-Wilke, 2006, Journal of veterinary medicine. B, Infectious diseases and veterinary public health.

Viral Antigen Distribution in the Central Nervous System of Cattle Persistently Infected with Bovine Viral Diarrhea Virus

G. Trautwein, B. Liess, A. Fernández, 1989, Veterinary pathology.

Experimental intrauterine infection of adult BALB/c mice with Cryptosporidium sp

J. Pohlenz, D. Woodmansee, E. Liebler, 1986, Infection and immunity.

[Bovine cryptosporidiosis. Diagnosis and therapy].

J. Pohlenz, B. Nagy, 1982, Tierarztliche Praxis.

[The significance of bredavirus as a diarrhea agent in calf herds in Lower Saxony].

J. Pohlenz, M. Koopmans, E. Liebler, 1992, DTW. Deutsche tierarztliche Wochenschrift.

A morphological study of the replication of Breda virus (proposed family Toroviridae) in bovine intestinal cells.

J. Pohlenz, G. Woode, J. Fagerland, 1986, The Journal of general virology.

Comparative studies on three isolates of Breda virus of calves.

L. Saif, N. Winand, J. Pohlenz, 1985, American journal of veterinary research.

Cellular Lesions in Intestinal Mucosa of Gnotobiotic Calves Experimentally Infected with a New Unclassified Bovine Virus (Breda Virus)

N. Cheville, J. Pohlenz, G. Woode, 1984, Veterinary pathology.

[Cryptosporidiosis in humans and animals].

J. Pohlenz, 1987, DTW. Deutsche tierarztliche Wochenschrift.

Factors affecting motility and morphology of Cryptosporidium sporozoites in vitro.

H. Moon, E. C. Powell, J. Pohlenz, 1987, The Journal of protozoology.

Serotypes of bovine astrovirus

J. Pohlenz, G. Woode, E. Liebler, 1985, Journal of clinical microbiology.

Generalized AA-amyloidosis in Siberian Tigers (Panthera tigris altaica) with Predominant Renal Medullary Amyloid Deposition

R. Linke, M. Brügmann, J. Pohlenz, 1998, Veterinary pathology.

[Virological studies of the central nervous system of horse fetuses and findings in mares suffering from central nervous system disease following abortion caused by equine herpesvirus 1].

J. Pohlenz, U. Teichert, K. Petzoldt, 1972, Schweizer Archiv fur Tierheilkunde.

Modification of thyroid hormone and 9-cis retinoic acid signaling by overexpression of their cognate receptors using adenoviral vector

H. Seo, Y. Hayashi, Y. Murata, 1997, Molecular and Cellular Endocrinology.

Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

D. Luton, M. Polak, H. Krude, 2020, Thyroid : official journal of the American Thyroid Association.

Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.

C. Roth, G. Borck, U. Martiné, 2003, The Journal of clinical endocrinology and metabolism.

Porcine colonic lymphoglandular complex: distribution, structure, and epithelium.

D C Morfitt, D. Morfitt, J F Pohlenz, 1989, The American journal of anatomy.

Gut-associated Lymphoid Tissue in the Large Intestine of Calves. I. Distribution and Histology

G N Woode, E M Liebler, J F Pohlenz, 1988, Veterinary pathology.

Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.

R. Weiss, S. Refetoff, S. Kimura, 2002, The Journal of clinical investigation.

A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy.

O. Hiort, J. Pohlenz, W. Ahrens, 2003, European journal of endocrinology.

Mice deficient in the steroid receptor co‐activator 1 (SRC‐1) are resistant to thyroid hormone

R. Weiss, S. Refetoff, Bert W. O’Malley, 1999, The EMBO journal.

Uptake of colostral leukocytes in the intestinal tract of newborn calves.

E. Liebler-Tenorio, J. Pohlenz, G. Riedel-Caspari, 2002, Veterinary immunology and immunopathology.

Linking C5 Deficiency to an Exonic Splicing Enhancer Mutation

C. Burge, W. Fairbrother, D. Prawitt, 2005, The Journal of Immunology.

Linking C5 deficiency to an exonic splicing enhancer mutation

C. Burge, W. Fairbrother, D. Prawitt, 2009, The Journal of Immunology.

Non-immune goiter and hypothyroidism in a 19-week fetus: a plea for conservative treatment.

D. Francoeur, J. Deladoëy, N. Alos, 2010, The Journal of pediatrics.

Intrauterine therapy of goitrous hypothyroidism in a boy with a new compound heterozygous mutation (Y453D and C800R) in the thyroid peroxidase gene. A long-term follow-up.

W. Holzgreve, J. Pohlenz, Kirsten Börgel, 2005, American journal of obstetrics and gynecology.

Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism

M. Schlesner, G. Rappold, G. Hoffmann, 2020, Hormone Research in Paediatrics.

A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle

C. Drögemüller, O. Distl, T. Leeb, 2002, Journal of Molecular Medicine.

Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH.

Jun Xie, J. Parma, P. Beck‐Peccoz, 1997, The Journal of clinical endocrinology and metabolism.

A case report: encephalitis in lions. Pathological and virological findings.

U. Truyen, N. Stockhofe-Zurwieden, J. Pohlenz, 1990, DTW. Deutsche tierarztliche Wochenschrift.

Autonomous thyroid adenoma: only an adulthood disease?

T. Musholt, N. Pfarr, M. Pohl, 2009, The Journal of pediatrics.

Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations in thyroid hormone receptor beta or alpha genes.

P. Macchia, R. Weiss, S. Refetoff, 2000, The Journal of clinical endocrinology and metabolism.

Thyrotropin Regulation by Thyroid Hormone in Thyroid Hormone Receptor β-Deficient Mice.

D. Forrest, T. Curran, R. Weiss, 1997, Endocrinology.

Selective pituitary resistance to thyroid hormone produced by expression of a mutant thyroid hormone receptor beta gene in the pituitary gland of transgenic mice.

Y. Hayashi, R. Weiss, S. Refetoff, 1998, Biochemical and biophysical research communications.

Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient mice.

D. Forrest, T. Curran, R. Weiss, 1997, Endocrinology.

Thyroid function tests in three affected members of a family with generalised resistance to thyroid hormone

A. Winterpacht, B. Zabel, S. Wirth, 2022 .

Studies of the detection of Listeria monocytogenes by culture and PCR in cerebrospinal fluid samples from ruminants with listeric encephalitis.

K. Jaton, J. Billé, M. Peters, 1995, Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B.

Gut-associated Lymphoid Tissue in the Large Intestine of Calves. II. Electron Microscopy

N. Cheville, J. Pohlenz, E. Liebler, 1988, Veterinary pathology.

Morphology of starch digestion in the horse.

E. Kienzle, J. Pohlenz, S. Radicke, 1997, Zentralblatt für Veterinärmedizin Reihe A.

Microscopy of starch digestion in the horse

E. Kienzle, J. Pohlenz, S. Radicke, 1998 .

Genotype-Phenotype Correlations in Pompe Disease

H. Runz, E. Mengel, R. Hartung, 2011 .

Two cases of thyroid dysgenesis caused by different novel PAX8 mutations in the DNA-binding region: in vitro studies reveal different pathogenic mechanisms.

H. Dörr, S. Refetoff, H. Grasberger, 2012, Thyroid : official journal of the American Thyroid Association.

Uterine and placental alterations in pregnant sows associated with the porcine epidemic abortion and respiratory syndrome (PEARS).

N. Stockhofe-Zurwieden, J. Pohlenz, J. Chávez, 1993, Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B.

[Infection with Bacillus piliformis (Tyzzer's disease) in foals].

H. Gerhards, N. Stockhofe-Zurwieden, J. Pohlenz, 1993, Schweizer Archiv fur Tierheilkunde.

Leukopenia and thrombocytopenia in pigs after infection with bovine viral diarrhoea virus-2 (BVDV-2).

D. Goovaerts, E. Liebler-Tenorio, B. Makoschey, 2002, DTW. Deutsche tierarztliche Wochenschrift.

Experimental mucosal disease of cattle: changes in cell proliferation in lymphoid tissues and intestinal epithelium.

E. Liebler-Tenorio, J. Pohlenz, 1997, Journal of comparative pathology.

Ultrastructural changes in follicles of small-intestinal aggregated lymphoid nodules in early and advanced phases of experimentally induced mucosal diseases in calves.

E. Liebler-Tenorio, J. Pohlenz, U. Teichmann, 2000, American Journal of Veterinary Research.

Reproduction of mucosal disease with cytopathogenic bovine viral diarrhoea virus selected in vitro

V. Moennig, B. Liess, J. Pohlenz, 1990, Veterinary Record.

Ultrastructure of the Intestinal Mucosa in Pigs Experimentally Inoculated with an Edema Disease-Producing Strain of Escherichia coli (0139:K12:H1)

J. Pohlenz, H. Bertschinger, S. Methiyapun, 1984, Veterinary pathology.

Canine dysautonomia resembling the Key-Gaskell syndrome in Germany

J. Pohlenz, C. Schulze, H. Schanen, 1997, Veterinary Record.

Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.

D. Bercovich, D. Bernard, Y. Tenenbaum‐Rakover, 2016, Thyroid : official journal of the American Thyroid Association.

A further case of brain-lung-thyroid syndrome with deletion proximal to NKX2-1.

I. Horrocks, M. Donaldson, J. Jones, 2017, European journal of medical genetics.

A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations

H. Runz, N. Karabul, M. Beck, 2012, Orphanet Journal of Rare Diseases.

Total serum bile acid concentrations in dairy cows with fatty liver and liver failure.

J. Rehage, N. Stockhofe-Zurwieden, C. Meier, 1999, DTW. Deutsche tierarztliche Wochenschrift.

A single copy of the recently identified dual oxidase maturation factor (DUOXA) 1 gene produces only mild transient hypothyroidism in a patient with a novel biallelic DUOXA2 mutation and monoallelic DUOXA1 deletion.

S. Refetoff, S. Heger, H. Grasberger, 2011, The Journal of clinical endocrinology and metabolism.

Resistance to thyroid hormone caused by two mutant thyroid hormone receptors beta, R243Q and R243W, with marked impairment of function that cannot be explained by altered in vitro 3,5,3'-triiodothyroinine binding affinity.

Y. Hayashi, S. Refetoff, J. Pohlenz, 1997, The Journal of clinical endocrinology and metabolism.

Identification of leucocyte surface antigens in paraffin- embedded bovine tissues using a modified formalin dichromate fixation

P. Wohlsein, B. Rathkolb, J. Pohlenz, 1997, The Histochemical Journal.

Congenital primary hypothyroidism in a turkish family caused by a homozygous nonsense mutation (R609X) in the thyrotropin receptor gene.

B. Hauffa, N. Pfarr, A. Richter-Unruh, 2004, Thyroid : official journal of the American Thyroid Association.

Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene.

R. Weiss, S. Refetoff, P. Sadow, 2001, The Journal of pediatrics.

Chronic Grass Sickness (equine dysautonomia) in a 21years old lcelandic mare on a north frisian island

J. Pohlenz, M. Venner, C. Schulze, 1997 .

Role of nutrition in the pathogenesis of porcine Escherichia coli enterotoxaemia.

J. Pohlenz, H. Bertschinger, H. Jucker, 1983, Annales de recherches veterinaires. Annals of veterinary research.

M cells in the rectum of calves.

J. Pohlenz, M. Paar, E. Liebler, 1991, Research in veterinary science.

[Disseminated intravascular coagulation and hyperfibrinolysis in dogs with metastasizing mammary carcinoma].

P. Wohlsein, R. Mischke, J. Pohlenz, 1998, Schweizer Archiv fur Tierheilkunde.

[Studies on the mastitis-metritis-agalactia syndrome (milk fever) in sows. III. Galactogenic induction of Klebsiella-induced mastitis].

J. Pohlenz, H. Bertschinger, D. M. Middleton-Williams, 1977, Schweizer Archiv fur Tierheilkunde.

Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid Syndrome

S. Refetoff, H. Grasberger, J. Pohlenz, 2017, Experimental and Clinical Endocrinology & Diabetes.

Clinical features of pediatric Graves’ orbitopathy

S. Pitz, J. Pohlenz, J. Eha, 2010, International Ophthalmology.

Mutations in the sodium/iodide symporter (NIS) gene as a cause for iodide transport defects and congenital hypothyroidism.

S. Refetoff, J. Pohlenz, 1999, Biochimie.

Congenital hypotrichosis and oligodontia in cattle

C. Drögemüller, O. Distl, T. Leeb, 2003 .

Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene.

J. Gross, S. Refetoff, M. Knobel, 1997, Biochemical and biophysical research communications.

Bovine spongiform encephalopathy in Germany.

M. Groschup, U. Truyen, E. Kaiser, 1994, Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B.

Ultrastructural study of the uptake of ferritin by M cells in the follicle-associated epithelium in the small and large intestines of pigs.

J. Pohlenz, C. Lemke, E. Liebler, 1995, American journal of veterinary research.

New point mutation (R243W) in the hormone binding domain of the c‐erbA β1 gene in a family with generalized resistance to thyroid hormone

A. Winterpacht, B. Zabel, S. Wirth, 1996, Human mutation.

Renal Coccidiosis with Cystic Tubular Dilatation in Four Bats

M. Brügmann, J. Pohlenz, A. D. Gruber, 1996, Veterinary Pathology-Supplement.

[Central nervous disorder in a horse caused by nematodes of the genus Micronema (Rhabditida)].

J. Eckert, J. Pohlenz, H. Minder, 1981, Berliner und Münchener tierärztliche Wochenschrift (1946).

A de novo mutation in an already mutant nucleotide of the thyroid hormone receptor beta gene perpetuates resistance to thyroid hormone.

A. Verloes, R. Weiss, S. Refetoff, 2005, The Journal of clinical endocrinology and metabolism.

Phenotypic variability in patients with generalised resistance to thyroid hormone.

A. Winterpacht, B. Zabel, S. Wirth, 1995, Journal of medical genetics.

[Calcinosis in sheep].

J. Pohlenz, S. de Barros, C. Santiago, 1970, Deutsche tierarztliche Wochenschrift.

Resistance to Thyroid Hormone in the Absence of Mutations in the Thyroid Hormone Receptor Genes

R. Weiss, S. Refetoff, P. Sadow, 2000 .

A novel homozygous mutation in the Solute Carrier Family 26 Member 7 (SLC26A7) gene causes thyroid dyshormonogenesis in a girl with congenital hypothyroidism.

J. Pohlenz, P. Hermanns, Charlotte Claßen, 2020, Thyroid : official journal of the American Thyroid Association.

Manifestation of Diabetes Mellitus Type 1: A Questionnaire to Evaluate the Acceptance of Initial Intravenous Therapy

D. Kieninger-Baum, J. Pohlenz, Katrin Steul, 2014 .

Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis.

S. Refetoff, H. Grasberger, J. Pohlenz, 2011, The Journal of clinical endocrinology and metabolism.

Inheritance and genetic mapping of the Campus syndrome (CPS): a high-frequency tremor disease in pigs.

B. Harlizius, D. Simon, D. Waberski, 1999, The Journal of heredity.